Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles

ABSTRACT

Fungicidal mixture comprising substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles The present invention relates to fungicidal mixtures comprising at least one substituted 3-phenyl-5-(trifluoromethyl)-1,2,4-oxadiazoles (compounds I) and at least one active compound II in a weight ratio of from 100:1 to 1:100; to a method for controlling phytopathogenic harmful fungi using mixtures of at least one compound I and at least one compound II in a weight ratio of from 100:1 to 1:100; to the use of mixtures comprising compounds I and compounds II for controlling phytopathogenic harmful fungi; to agrochemical compositions comprising these mixtures; and to agrochemical compositions further comprising seed.

The present invention relates to a fungicidal mixture comprising, asactive components

-   1) at least one active compound of the formula I, or an N-oxide, or    an agriculturally useful salt thereof,

-   -   wherein:    -   W is —(C═O)—NR²-#, —(C═S)—NR²-#, —NR²—(C═O)-# or —NR²—(C═S)-#;        wherein # denotes the position, which is attached to the group        R¹;    -   R¹ is C₁-C₆-alkyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl,        C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxyimino-C₁-C₄-alkyl or        phenyl; wherein the phenyl ring is unsubstituted or substituted        with 1, 2, 3 or up to the maximum possible number of identical        or different radicals selected from the group consisting of        halogen, C₁-C₆-alkyl and C₁-C₆-alkoxy;    -   R² is hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,        C₁-C₆-alkoxy, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, and        C₃-C₅-cycloalkyl-C₁-C₄-alkyl; and wherein any of the aliphatic        or cyclic groups are unsubstituted or substituted with 1, 2, 3        or up to the maximum possible number of identical or different        radicals selected from the group consisting of halogen, hydroxy,        oxo, cyano, C₁-C₆-alkyl, C₁-C₆-alkoxy and C₃-C₈-cycloalkyl; or    -   R¹ and R² together with the nitrogen atom to which they are        bound form a saturated or partially unsaturated mono- or        bicyclic 3- to 7-membered heterocycle, wherein the heterocycle        includes beside one nitrogen atom and one or more carbon atoms        no further heteroatom or 1, 2 or 3 further heteroatoms        independently selected from N, O and S as ring member atoms; and        wherein one or two CH₂ groups of the heterocycle may be replaced        by one or two groups independently selected from the group of        C(═O) and C(═S); and wherein the heterocycle is unsubstituted or        carries 1, 2, 3, 4 or up to the maximum possible number of        identical or different radicals selected from the group        consisting of halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl,        C₁-C₆-alkoxy,    -   m is 0 or 1;    -   R³, R⁴ independently of each other are selected from the group        consisting of hydrogen, halogen, cyano, C₁-C₄-alkyl,        C₁-C₄-alkenyl, C₁-C₄-alkynyl, C₁-C₄-haloalkyl and C₁-C₄-alkoxy;    -   or R³ and R⁴ together with the carbon atom to which they are        bound form a cyclopropyl ring;    -   and as component

-   2) at least one active compound II selected from groups A) to O), or    an N-oxide, or an agriculturally useful salt thereof:

A) Respiration Inhibitors:

Inhibitors of complex III at Q_(o) site: azoxystrobin (A.1.1),coumethoxystrobin (A.1.2), coumoxystrobin (A.1.3), dimoxystrobin(A.1.4), enestroburin (A.1.5), fenaminstrobin (A.1.6),fenoxystrobin/flufenoxystrobin (A.1.7), fluoxastrobin (A.1.8),kresoxim-methyl (A.1.9), mandestrobin (A.1.10), metominostrobin(A.1.11), orysastrobin (A.1.12), picoxystrobin (A.1.13), pyraclostrobin(A.1.14), pyrametostrobin (A.1.15), pyraoxystrobin (A.1.16),trifloxystrobin (A.1.17),2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide(A.1.18), pyribencarb (A.1.19), triclopyricarb/chlorodincarb (A.1.20),famoxadone (A.1.21), fenamidone (A.1.21a),methyl-N-[2-[(1,4-dimethyl-5-phenyl-pyrazol-3-yl)oxylmethyl]phenyl]-N-methoxy-carbamate(A.1.22),1-[3-chloro-2-[[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.23),1-[3-bromo-2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.24),1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one(A.1.25),1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one(A.1.26),1-[2-[[1-(2,4-dichlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one(A.1.27),1-[2-[[4-(4-chlorophenyl)thiazol-2-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one(A.1.28),1-[3-chloro-2-[[4-(p-tolyl)thiazol-2-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.29),1-[3-cyclopropyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]-methyl]phenyl]-4-methyl-tetrazol-5-one(A.1.30),1-[3-(difluoromethoxy)-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one(A.1.31),1-methyl-4-[3-methyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one(A.1.32),1-methyl-4-[3-methyl-2-[[1-[3-(trifluoromethyl)phenyl]-ethylideneamino]oxymethyl]phenyl]tetrazol-5-one(A.1.33),(Z,2E)-5-[1-(2,4-dichlorophenyl)pyrazol-3-yl]-oxy-2-methoxyimino-N,3-dimethyl-pent-3-enamide(A.1.34),(Z,2E)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-N,3-dimethyl-pent-3-enamide(A.1.35), pyriminostrobin (A.1.36), bifujunzhi (A.1.37),2-(ortho-((2,5-dimethylphenyl-oxymethylen)phenyl)-3-methoxy-acrylic acidmethylester (A.1.38);

Inhibitors of complex III at Q_(i) site: cyazofamid (A.2.1), amisulbrom(A.2.2),[(6S,7R,8R)-8-benzyl-3-[(3-hydroxy-4-methoxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]2-methylpropanoate (A.2.3), fenpicoxamid (A.2.4),[(6S,7R,8R)-8-benzyl-3-[[4-methoxy-3-(propanoyloxymethoxy)pyridine-2-carbonyl]amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]2-methylpropanoate (A.2.5), florylpicoxamid (A.2.6);

Inhibitors of complex II: benodanil (A.3.1), benzovindiflupyr (A.3.2),bixafen (A.3.3), boscalid (A.3.4), carboxin (A.3.5), fenfuram (A.3.6),fluopyram (A.3.7), flutolanil (A.3.8), fluxapyroxad (A.3.9), furametpyr(A.3.10), isofetamid (A.3.11), isopyrazam (A.3.12), mepronil (A.3.13),oxycarboxin (A.3.14), penflufen (A.3.15), penthiopyrad (A.3.16),pydiflumetofen (A.3.17),N-[2-(3,4-difluorophenyl)phenyl]-3-(trifluoromethyl)pyrazine-2-carboxamide(A.3.18), sedaxane (A.3.19), tecloftalam (A.3.20), thifluzamide(A.3.21),3-(difluoromethyl)-1-methyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.22),3-(trifluoromethyl)-1-methyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.23),1,3-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.24),3-(trifluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.25),1,3,5-trimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.26),3-(difluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.27),3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-indan-4-yl)-1-methyl-pyrazole-4-carboxamide(A.3.28),N-[2-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]-3-(difluoromethyl)-5-fluoro-1-methyl-pyrazole-4-carboxamide(A.3.29), methyl(E)-2-[2-[(5-cyano-2-methyl-phenoxy)methyl]phenyl]-3-methoxy-prop-2-enoate(A.3.30),N-[(5-chloro-2-isopropyl-phenyl)methyl]-N-cyclopropyl-3-(difluoromethyl)-5fluoro-1-methyl-pyrazole-4-carboxamide (A.3.31),2-(difluoromethyl)-N-(1,1,3-trimethyl-indan-4-yl)pyridine-3-carboxamide(A.3.32),2-(difluoromethyl)-N-[(3R)-1,1,3-trimethylindan-4-yl]pyridine-3-carboxamide(A.3.33),2-(difluoromethyl)-N-[(3S)3-ethyl-1,1-dimethyl-indan-4-yl]pyridine-3-carboxamide(A.3.34),2-(difluoromethyl)-N-[(3R)-3-ethyl-1,1-dimethyl-indan-4-yl]pyridine-3-carboxamide(A.3.35),2-(difluoromethyl)-N-(1,1-dimethyl-3-propyl-indan-4-yl)pyridine-3-carboxamide(A.3.36),2-(difluoromethyl)-N-[(3R)-1,1-dimethyl-3-propyl-indan-4-yl]pyridine-3-carboxamide(A.3.37),2-(difluoromethyl)-N-(3-isobutyl-1,1-dimethyl-indan-4-yl)pyridine-3-carboxamide(A.3.38), 2-(difluoromethyl)-N-[(3R)-3-isobutyl-1,1-dimethyl-indan-4yl]pyridine-3-carboxamide (A.3.39);

Other respiration inhibitors: diflumetorim (A.4.1); nitrophenylderivates: binapacryl (A.4.2), dinobuton (A.4.3), dinocap (A.4.4),fluazinam (A.4.5), meptyldinocap (A.4.6), ferimzone (A.4.7); organometalcompounds: fentin salts, e. g. fentin-acetate (A.4.8), fentin chloride(A.4.9) or fentin hydroxide (A.4.10); ametoctradin (A.4.11); silthiofam(A.4.12);

B) Sterol Biosynthesis Inhibitors (SBI Fungicides)

C14 demethylase inhibitors: triazoles: azaconazole (B.1.1), bitertanol(B.1.2), bromuconazole (B.1.3), cyproconazole (B.1.4), difenoconazole(B.1.5), diniconazole (B.1.6), diniconazole-M (B.1.7), epoxiconazole(B.1.8), fenbuconazole (B.1.9), fluquinconazole (B.1.10), flusilazole(B.1.11), flutriafol (B.1.12), hexaconazole (B.1.13), imibenconazole(B.1.14), ipconazole (B.1.15), metconazole (B.1.17), myclobutanil(B.1.18), oxpoconazole (B.1.19), paclobutrazole (B.1.20), penconazole(B.1.21), propiconazole (B.1.22), prothioconazole (B.1.23), simeconazole(B.1.24), tebuconazole (B.1.25), tetraconazole (B.1.26), triadimefon(B.1.27), triadimenol (B.1.28), triticonazole (B.1.29), uniconazole(B.1.30),1-[re(2,3R)-3-(2-chloro-phenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-5-thiocyanato-1H-[1,2,4]triazole(B.1.31), 2-[rel(2S,3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-2H-[1,2,4]triazole-3-thiol(B.1.32),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)pentan-2-ol(B.1.33),1-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-cyclopropyl-2-(1,2,4-triazol-1-yl)ethanol(B.1.34),2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.35),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.36), ipfentrifluconazole (B.1.37), mefentrifluconazole (B.1.38),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.39),2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)pentan-2-ol(B.1.40),2-[4-(4-fluorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol(B.1.41),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)pent-3-yn-2-ol(B.1.42),2-(chloromethyl)-2-methyl-5-(p-tolylmethyl)-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol(B.1.43); imidazoles: imazalil (B.1.44), pefurazoate (B.1.45),prochloraz (B.1.46), triflumizol (B.1.47); pyrimidines, pyridines andpiperazines: fenarimol (B.1.49), pyrifenox (B.1.50), triforine (B.1.51),[3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluorophenyl)isoxazol-4-yl]-(3-pyridyl)methanol(B.1.52);

Delta14-reductase inhibitors: aldimorph (B.2.1), dodemorph (B.2.2),dodemorph-acetate (B.2.3), fenpropimorph (B.2.4), tridemorph (B.2.5),fenpropidin (B.2.6), piperalin (B.2.7), spiroxamine (B.2.8);

Inhibitors of 3-keto reductase: fenhexamid (B.3.1);

Other Sterol biosynthesis inhibitors: chlorphenomizole (B.4.1);

C) Nucleic Acid Synthesis Inhibitors

Phenylamides or acyl amino acid fungicides: benalaxyl (C.1.1),benalaxyl-M (C.1.2), kiralaxyl (C.1.3), metalaxyl (C.1.4), metalaxyl-M(C.1.5), ofurace (C.1.6), oxadixyl (C.1.7);

Other nucleic acid synthesis inhibitors: hymexazole (C.2.1), octhilinone(C.2.2), oxolinic acid (C.2.3), bupirimate (C.2.4), 5-fluorocytosine(C.2.5), 5-fluoro-2-(p-tolylmethoxy)pyrimidin-4-amine (C.2.6),5-fluoro-2-(4-fluorophenylmethoxy)pyrimidin-4-amine (C.2.7),5-fluoro-2-(4-chlorophenylmethoxy)pyrimidin-4 amine (C.2.8);

D) Inhibitors of Cell Division and Cytoskeleton

Tubulin inhibitors: benomyl (D.1.1), carbendazim (D.1.2), fuberidazole(D1.3), thiabendazole (D.1.4), thiophanate-methyl (D.1.5),3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenyl-pyridazine (D.1.6),3-chloro-6-methyl-5-phenyl-4-(2,4,6-trifluorophenyl)pyridazine (D.1.7),N-ethyl-2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]butanamide (D.1.8),N-ethyl-2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methylsulfanyl-acetamide(D.1.9),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-fluoroethyl)butanamide(D.1.10),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-fluoroethyl)-2-methoxy-acetamide(D.1.11), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-propyl-butanamide(D.1.12),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methoxy-N-propyl-acetamide(D.1.13),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methylsulfanyl-N-propyl-acetamide(D.1.14),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-fluoroethyl)-2-methylsulfanyl-acetamide(D.1.15),4-(2-bromo-4-fluoro-phenyl)-N-(2-chloro-6-fluoro-phenyl)-2,5-dimethyl-pyrazol-3-amine(D.1.16);

Other cell division inhibitors: diethofencarb (D.2.1), ethaboxam(D.2.2), pencycuron (D.2.3), fluopicolide (D.2.4), zoxamide (D.2.5),metrafenone (D.2.6), pyriofenone (D.2.7);

E) Inhibitors of Amino Acid and Protein Synthesis

Methionine synthesis inhibitors: cyprodinil (E.1.1), mepanipyrim(E.1.2), pyrimethanil (E.1.3);

Protein synthesis inhibitors: blasticidin-S(E.2.1), kasugamycin (E.2.2),kasugamycin hydrochloride-hydrate (E.2.3), mildiomycin (E.2.4),streptomycin (E.2.5), oxytetracyclin (E.2.6);

F) Signal Transduction Inhibitors

MAP/histidine kinase inhibitors: fluoroimid (F.1.1), iprodione (F.1.2),procymidone (F.1.3), vinclozolin (F.1.4), fludioxonil (F.1.5);

G protein inhibitors: quinoxyfen (F.2.1);

G) Lipid and Membrane Synthesis Inhibitors

Phospholipid biosynthesis inhibitors: edifenphos (G.1.1), iprobenfos(G.1.2), pyrazophos (G.1.3), isoprothiolane (G.1.4);

Lipid peroxidation: dicloran (G.2.1), quintozene (G.2.2), tecnazene(G.2.3), tolclofos-methyl (G.2.4), biphenyl (G.2.5), chloroneb (G.2.6),etridiazole (G.2.7);

Phospholipid biosynthesis and cell wall deposition: dimethomorph(G.3.1), flumorph (G.3.2), mandipropamid (G.3.3), pyrimorph (G.3.4),benthiavalicarb (G.3.5), iprovalicarb (G.3.6), valifenalate (G.3.7);

Compounds affecting cell membrane permeability and fatty acides:propamocarb (G.4.1);

Inhibitors of oxysterol binding protein: oxathiapiprolin (G.5.1),2-{3-[2-(1-{[3,5-bis(difluoro-methyl-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-phenylmethanesulfonate (G.5.2),2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-acetyl}piperidin-4-yl)1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenylmethane-sulfonate (G.5.3),4-[1-[2-[3-(difluoromethyl)-5-methyl-pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.4),4-[1-[2-[3,5-bis(difluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.5),4-[1-[2-[3-(difluoromethyl)-5-(tri-fluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.6),4-[1-[2-[5-cyclopropyl-3-(difluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.7),4-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.8),4-[1-[2-[5-(difluoromethyl)-3-(trifluoro-methyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.9),4-[1-[2-[3,5-bis(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.10),(4-[1-[2-[5-cyclopropyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.11);

H) Inhibitors with Multi Site Action

Inorganic active substances: Bordeaux mixture (H.1.1), copper (H.1.2),copper acetate (H.1.3), copper hydroxide (H.1.4), copper oxychloride(H.1.5), basic copper sulfate (H.1.6), sulfur (H.1.7);

Thio- and dithiocarbamates: ferbam (H.2.1), mancozeb (H.2.2), maneb(H.2.3), metam (H.2.4), metiram (H.2.5), propineb (H.2.6), thiram(H.2.7), zineb (H.2.8), ziram (H.2.9);

Organochlorine compounds: anilazine (H.3.1), chlorothalonil (H.3.2),captafol (H.3.3), captan (H.3.4), folpet (H.3.5), dichlofluanid (H.3.6),dichlorophen (H.3.7), hexachlorobenzene (H.3.8), pentachlorphenole(H.3.9) and its salts, phthalide (H.3.10), tolylfluanid (H.3.11);

Guanidines and others: guanidine (H.4.1), dodine (H.4.2), dodine freebase (H.4.3), guazatine (H.4.4), guazatine-acetate (H.4.5), iminoctadine(H.4.6), iminoctadine-triacetate (H.4.7), iminoctadine-tris(albesilate)(H.4.8), dithianon (H.4.9),2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c′]dipyrrole-1,3,5,7(2H,6H)-tetraone(H.4.10);

I) Cell Wall Synthesis Inhibitors

Inhibitors of glucan synthesis: validamycin (I.1.1), polyoxin B (I.1.2);

Melanin synthesis inhibitors: pyroquilon (I.2.1), tricyclazole (I.2.2),carpropamid (I.2.3), dicyclomet (I.2.4), fenoxanil (I.2.5);

J) Plant Defence Inducers

Acibenzolar-S-methyl (J.1.1), probenazole (J.1.2), isotianil (J.1.3),tiadinil (J.1.4), prohexadione-calcium (J.1.5); phosphonates: fosetyl(J.1.6), fosetyl-aluminum (J.1.7), phosphorous acid and its salts(J.1.8), potassium or sodium bicarbonate (J.1.9),4-cyclopropyl-N-(2,4-dimethoxyphenyl)thiadiazole-5-carboxamide (J.1.10),calcium phosphonate (J.1.11), potassium phosphonate (J.1.12);

K) Unknown Mode of Action

Bronopol (K.1.1), chinomethionat (K.1.2), cyflufenamid (K.1.3),cymoxanil (K.1.4), dazomet (K.1.5), debacarb (K.1.6), diclocymet(K.1.7), diclomezine (K.1.8), difenzoquat (K.1.9),difenzoquat-methylsulfate (K.1.10), diphenylamin (K.1.11), fenitropan(K.1.12), fenpyrazamine (K.1.13), flumetover (K.1.14), flusulfamide(K.1.15), flutianil (K.1.16), harpin (K.1.17), methasulfocarb (K.1.18),nitrapyrin (K.1.19), nitrothal-isopropyl (K.1.20), tolprocarb (K.1.21),oxincopper (K.1.22), proquinazid (K.1.23), tebufloquin (K.1.24),tecloftalam (K.1.25), triazoxide (K.1.26),N′-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methylformamidine (K.1.27),N′-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methylformamidine (K.1.28),N′-[4-[[3-[(4-chorophenyl)methyl]-1,2,4-thiadiazo-5-yl]oxy]-2,5-dimethyl-phenyl]-N-ethyl-N-methyl-formamidine(K.1.29),N′-(5-bromo-6-indan-2-yloxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine(K.1.30),N′-[5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methyl-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.31),N′-[5-bromo-6-(4-isopropylcyclohexoxy)-2-methyl-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.32),N′-[5-bromo-2-methyl-6-(1-phenylethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.33),N′-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methylformamidine (K.1.34),N′-(5-difluoromethyl-2-methyl-4-(3-trimethylsianyl-propoxy)-phenyl)-N-ethyl-N-methylformamidine (K.1.35),2-(4-chloro-phenyl)-N-[4-(3,4-dimethoxy-phenyl)-isoxazol-5-yl]-2-prop-2-ynyloxy-acetamide(K.1.36),3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine(pyrisoxazole) (K.1.37),3-[5-(4-methylphenyl)-2,3-dimethyl-isoxazolidin-3 yl]-pyridine (K.1.38),5-chloro-1-(4,6-dimethoxy-pyrimidin-2-yl)-2-methyl-1H-benzoimidazole(K.1.39), ethyl (Z)-3-amino-2-cyano-3-phenyl-prop-2-enoate (K.1.40),picarbutrazox (K.1.41), pentylN-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carba-mate(K.1.42), but-3-ynylN-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carbamate(K.1.43),2-[2-[(7,8-difluoro-2-methyl-3-quinolyl)oxy]-6-fluoro-phenyl]propan-2-ol(K.1.44),2-[2-fluoro-6-[(8-fluoro-2-methyl-3-quinolyl)oxy]phen-yl]propan-2-ol(K.1.45),3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline(K.1.46), quinofumelin (K.1.47),3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline(K.1.48), 9-fluoro-2,2-dimethyl-5-(3-quinolyl)-3H-1,4-benzoxazepine(K.1.49), 2-(6-benzyl-2-pyridyl)quinazoline (K.1.50),2-[6-(3-fluoro-4-methoxy-phenyl)-5-methyl-2-pyridyl]quinazoline(K.1.51), dichlobentiazox (K.1.52),N′-(2,5-dimethyl-4-phenoxy-phenyl)-N-ethyl-N-methyl-formamidine(K.1.53),N′-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.54);

M) Growth Regulators

abscisic acid (M.1.1), amidochlor, ancymidol, 6-benzylaminopurine,brassinolide, butralin, chlormequat, chlormequat chloride, cholinechloride, cyclanilide, daminozide, dikegulac, dimethipin,2,6-dimethylpuridine, ethephon, flumetralin, flurprimidol, fluthiacet,forchlorfenuron, gibberellic acid, inabenfide, indole-3-acetic acid,maleic hydrazide, mefluidide, mepiquat, mepiquat chloride,naphthaleneacetic acid, N-6-benzyladenine, paclobutrazol, prohexadione,prohexadione-calcium, prohydrojasmon, thidiazuron, triapenthenol,tributyl phosphoro-trithioate, 2,3,5-tri-iodobenzoic acid,trinexapac-ethyl and uniconazole;

N) Herbicides from Classes N.1 to N.15

N.1 Lipid biosynthesis inhibitors: alloxydim (N.1.1), alloxydim-sodium(N.1.2), butroxydim (N.1.3), clethodim (N.1.4), clodinafop (N.1.5),clodinafop-propargyl (N.1.6), cycloxydim (N.1.7), cyhalofop (N.1.8),cyhalofop-butyl (N.1.9), diclofop(N.1.10), diclofop-methyl (N.1.11),fenoxaprop (N.1.12), fenoxaprop-ethyl (N.1.13), fenoxaprop-P (N.1.14),fenoxaprop-P-ethyl (N.1.15), fluazifop (N.1.16), fluazifop-butyl(N.1.17), fluazifop-P (N.1.18), fluazifop-P-butyl (N.1.19), haloxyfop(N.1.20), haloxyfop-methyl (N.1.21), haloxyfop-P (N.1.22),haloxyfop-P-methyl (N.1.23), metamifop (N.1.24), pinoxaden (N.1.25),profoxydim (N.1.26), propaquizafop (N.1.27), quizalofop (N.1.28),quizalofop-ethyl (N.1.29), quizalofop-tefuryl (N.1.30), quizalofop-P(N.1.31), quizalofop-P-ethyl (N.1.32), quizalofop-P-tefuryl (N.1.33),sethoxydim (N.1.34), tepraloxydim (N.1.35), tralkoxydim (N.1.36),4-(4′-chloro-4-cyclo¬propyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.37) CAS 1312337-72-6);4-(2′,4′-dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.38) CAS 1312337-45-3);4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.39) CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione((N.1.40) CAS 1312340-84-3);5-(acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.41) CAS 1312337-48-6);5-(acetyloxy)-4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(N.1.42);5-(acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.43) CAS 1312340-82-1);5-(acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.44) CAS 1033760-55-2);4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.45) CAS 1312337-51-1);4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (N.1.46);4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.47) CAS 1312340-83-2);4-(2′,4′-dichloro-4-ethyl,[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.48) CAS 1033760-58-5); benfuresate(N.1.49), butylate (N.1.50), cycloate (N.1.51), dalapon (N.1.52),dimepiperate (N.1.53), EPTC (N.1.54), esprocarb (N.1.55), ethofumesate(N.1.56), flupropanate (N.1.57), molinate (N.1.58), orbencarb (N.1.59),pebulate (N.1.60), prosulfocarb (N.1.61), TCA (N.1.62), thiobencarb(N.1.63), tiocarbazil (N.1.64), triallate (N.1.65) and vernolate(N.1.66);

N.2 ALS inhibitors: amidosulfuron (N.2.1), azimsulfuron (N.2.2),bensulfuron (N.2.3), bensulfuron-methyl (N.2.4), chlorimuron (N.2.5),chlorimuron-ethyl (N.2.6), chlorsulfuron (N.2.7), cinosulfuron (N.2.8),cyclosulfamuron (N.2.9), ethametsulfuron (N.2.10),ethametsulfuron-methyl (N.2.11), ethoxysulfuron (N.2.12), flazasulfuron(N.2.13), flucetosulfuron (N.2.14), flupyrsulfuron (N.2.15),flupyrsulfuron-methyl-sodium (N.2.16), foramsulfuron (N.2.17),halosulfuron (N.2.18), halosulfuron-methyl (N.2.19), imazosulfuron(N.2.20), iodosulfuron (N.2.21), iodosulfuron-methyl-sodium (N.2.22),iofensulfuron (N.2.23), iofensulfuron-sodium (N.2.24), mesosulfuron(N.2.25), metazosulfuron (N.2.26), metsulfuron (N.2.27),metsulfuron-methyl (N.2.28), nicosulfuron (N.2.29), orthosulfamuron(N.2.30), oxasulfuron (N.2.31), primisulfuron (N.2.32),primisulfuron-methyl (N.2.33), propyrisulfuron (N.2.34), prosulfuron(N.2.35), pyrazosulfuron (N.2.36), pyrazosulfuron-ethyl (N.2.37),rimsulfuron (N.2.38), sulfometuron (N.2.39), sulfometuron-methyl(N.2.40), sulfosulfuron (N.2.41), thifensulfuron (N.2.42),thifensulfuron-methyl (N.2.43), triasulfuron (N.2.44), tribenuron(N.2.45), tribenuronmethyl (N.2.46), trifloxysulfuron (N.2.47),triflusulfuron (N.2.48), triflusulfuron-methyl (N.2.49), tritosulfuron(N.2.50), imazamethabenz (N.2.51), imazamethabenz-methyl (N.2.52),imazamox (N.2.53), imazapic (N.2.54), imazapyr (N.2.55), imazaquin(N.2.56), imazethapyr (N.2.57); cloransulam (N.2.58), cloransulam-methyl(N.2.59), diclosulam (N.2.60), flumetsulam (N.2.61), florasulam(N.2.62), metosulam (N.2.63), penoxsulam (N.2.64), pyrimisulfan (N.2.65)and pyroxsulam (N.2.66); bispyribac (N.2.67), bispyribac-sodium(N.2.68), pyribenzoxim (N.2.69), pyriftalid (N.2.70), pyriminobac(N.2.71), pyriminobac-methyl (N.2.72), pyrithiobac (N.2.73),pyrithiobac-sodium (N.2.74),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid-1-methyl¬ethyl ester ((N.2.75) CAS 420138-41-6),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]¬methyl]amino]-benzoicacid propyl ester ((N.2.76) CAS 420138-40-5),N-(4-bromophenyl)-2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]benzenemethanamine((N.2.77) CAS 420138-01-8); flucarbazone (N.2.78), flucarbazone-sodium(N.2.79), propoxycarbazone (N.2.80), propoxycarbazone-sodium (N.2.81),thiencarbazone (N.2.82), thiencarbazone-methyl (N.2.83), triafamone(N.2.84);

N.3 Photosynthesis inhibitors: amicarbazone (N.3.1); chlorotriazine(N.3.2); ametryn (N.3.3), atrazine (N.3.4), chloridazone (N.3.5),cyanazine (N.3.6), desmetryn (N.3.7), dimethametryn (N.3.8), hexazinone(N.3.9), metribuzin (N.3.10), prometon (N.3.11), prometryn (N.3.12),pro-pazine (N.3.13), simazine (N.3.14), simetryn (N.3.15), terbumeton(N.3.16), terbuthylazin (N.3.17), terbutryn (N.3.18), trietazin(N.3.19); chlorobromuron (N.3.20), chlorotoluron (N.3.21), chloroxuron(N.3.22), dimefuron (N.3.23), diuron (N.3.24), fluometuron (N.3.25),isoproturon (N.3.26), isouron (N.3.27), linuron (N.3.28), metamitron(N.3.29), methabenzthiazuron (N.3.30), metobenzuron (N.3.31), metoxuron(N.3.32), monolinuron (N.3.33), neburon (N.3.34), siduron (N.3.35),tebuthiuron (N.3.36), thiadiazuron (N.3.37), desmedipham (N.3.38),karbutilat (N.3.39), phenmedipham (N.3.40), phenmedipham-ethyl (N.3.41),bromofenoxim (N.3.42), bromoxynil (N.3.43) and its salts and esters,ioxynil (N.3.44) and its salts and esters, bromacil (N.3.45), lenacil(N.3.46), terbacil (N.3.47), bentazon (N.3.48), bentazon-sodium(N.3.49), pyridate (N.3.50), pyridafol (N.3.51), pentanochlor (N.3.52),propanil (N.3.53); diquat (N.3.54), diquat-dibromide (N.3.55), paraquat(N.3.56), paraquat-dichloride (N.3.57), paraquat-dimetilsulfate(N.3.58);

N.4 protoporphyrinogen-IX oxidase inhibitors: acifluorfen (N.4.1),acifluorfen-sodium (N.4.2), azafenidin (N.4.3), bencarbazone (N.4.4),benzfendizone (N.4.5), bifenox (N.4.6), butafenacil (N.4.7),carfentrazone (N.4.8), carfentrazone-ethyl (N.4.9), chlormethoxyfen(N.4.10), cinidon-ethyl (N.4.11), fluazolate (N.4.12), flufenpyr(N.4.13), flufenpyr-ethyl (N.4.14), flumiclorac (N.4.15),flumiclorac-pentyl (N.4.16), flumioxazin (N.4.17), fluoroglycofen(N.4.18), fluoroglycofen-ethyl (N.4.19), fluthiacet (N.4.20),fluthiacet-methyl (N.4.21), fomesafen (N.4.22), halosafen (N.4.23),lactofen (N.4.24), oxadiargyl (N.4.25), oxadiazon (N.4.26), oxyfluorfen(N.4.27), pentoxazone (N.4.28), profluazol (N.4.29), pyraclonil(N.4.30), pyraflufen (N.4.31), pyraflufen-ethyl (N.4.32), saflufenacil(N.4.33), sulfentrazone (N.4.34), thidiazimin (N.4.35), tiafenacil(N.4.36), trifludimoxazin (N.4.37), ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate((N.4.38) CAS 353292-31-6),N-ethyl-3-(2,6-dichloro-4-trifluoro-methylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.39) CAS 452098-92-9), Ntetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.40) CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethyl¬phenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.41) CAS 452099-05-7), Ntetrahydro¬furfuryl-3-(2-chloro-6-fluoro-4-trifluoro¬methylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.42) CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione((N.4.43) CAS 451484-50-7),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione((N.4.44) CAS 1300118-96-0),1-methyl-6-trifluoro¬methyl-3-(2,2,7-tri-fluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione((N.4.45) CAS 1304113-05-0), methyl(E)-4-[2-chloro-5-[4-chloro-5-(difluoromethoxy)-1H-methyl-pyrazol-3-yl]-4-fluoro-phenoxy]-3-methoxy-but-2-enoate((N.4.46) CAS 948893-00-3),3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione((N.4.47) CAS 212754-02-4);

N.5 Bleacher herbicides: beflubutamid (N.5.1), diflufenican (N.5.2),fluridone (N.5.3), flurochloridone (N.5.4), flurtamone (N.5.5),norflurazon (N.5.6), picolinafen (N.5.7),4-(3-trifluoromethyl¬phenoxy)-2-(4-trifluoromethylphenyl)¬pyrimidine((N.5.8) CAS 180608-33-7); benzobicyclon (N.5.9), benzofenap (N.5.10),bicyclopyrone (N.5.11), clomazone (N.5.12), fenquintrione (N.5.13),isoxaflutole (N.5.14), mesotrione (N.5.15), pyrasulfotole (N.5.16),pyrazolynate (N.5.17), pyrazoxyfen (N.5.18), sulcotrione (N.5.19),tefuryltrione (N.5.20), tembotrione (N.5.21), tolpyralate (N.5.22),topramezone (N.5.23); aclonifen (N.5.24), amitrole (N.5.25), flumeturon(N.5.26);

N.6 EPSP synthase inhibitors: glyphosate (N.6.1),glyphosate-isopropylammonium (N.6.2), glyposate-potassium (N.6.3),glyphosate-trimesium (sulfosate) (N.6.4);

N.7 Glutamine synthase inhibitors: bilanaphos (bialaphos) (N.7.1),bilanaphos-sodium (N.7.2), glufosinate (N.7.3), glufosinate-P (N.7.4),glufosinate-ammonium (N.7.5);

N.8 DHP synthase inhibitors: asulam (N.8.1);

N.9 Mitosis inhibitors: benfluralin (N.9.1), butralin (N.9.2),dinitramine (N.9.3), ethalfluralin (N.9.4), fluchloralin (N.9.5),oryzalin (N.9.6), pendimethalin (N.9.7), prodiamine (N.9.8), trifluralin(N.9.9); amiprophos (N.9.10), amiprophos-methyl (N.9.11), butamiphos(N.9.12); chlorthal (N.9.13), chlorthal-dimethyl (N.9.14), dithiopyr(N.9.15), thiazopyr (N.9.16), propyzamide (N.9.17), tebutam (N.9.18);carbetamide (N.9.19), chlorpropham (N.9.20), flamprop (N.9.21),flamprop-isopropyl (N.9.22), flamprop-methyl (N.9.23),flamprop-M-isopropyl (N.9.24), flamprop-M-methyl (N.9.25), propham(N.9.26);

N.10 VLCFA inhibitors: acetochlor (N.10.1), alachlor (N.10.2), butachlor(N.10.3), dimethachlor (N.10.4), dimethenamid (N.10.5), dimethenamid-P(N.10.6), metazachlor (N.10.7), metolachlor (N.10.8),metolachlor-S(N.10.9), pethoxamid (N.10.10), pretilachlor (N.10.11),propachlor (N.10.12), propisochlor (N.10.13), thenylchlor (N.10.14),flufenacet (N.10.15), mefenacet (N.10.16), diphenamid (N.10.17),naproanilide (N.10.18), napropamide (N.10.19), napropamide-M (N.10.20),fentrazamide (N.10.21), anilofos (N.10.22), cafenstrole (N.10.23),fenoxasulfone (N.10.24), ipfencarbazone (N.10.25), piperophos (N.10.26),pyroxasulfone (N.10.27), isoxazoline compounds of the formulae II.1,II.2, II.3, II.4, II.5, II.6, II.7, II.8 and II.9

N.11 Cellulose biosynthesis inhibitors: chlorthiamid (N.11.1),dichlobenil (N.11.2), flupoxam (N.11.3), indaziflam (N.11.4), isoxaben(N.11.5), triaziflam (N.11.6),1-cyclohexyl-5-pentafluorphenyloxy-14-[1,2,4,6]thiatriazin-3-ylamine((N.11.7) CAS 175899-01-1);

N.12 Decoupler herbicides: dinoseb (N.12.1), dinoterb (N.12.2), DNOC(N.12.3) and its salts;

N.13 Auxinic herbicides: 2,4-D (N.13.1) and its salts and esters,clacyfos (N.13.2), 2,4-DB (N.13.3) and its salts and esters,aminocyclopyrachlor (N.13.4) and its salts and esters, aminopyralid(N.13.5) and its salts such as aminopyralid-dimethylammonium (N.13.6),aminopyralid-tris(2-hydroxypropyl)ammonium (N.13.7) and its esters,benazolin (N.13.8), benazolin-ethyl (N.13.9), chloramben (N.13.10) andits salts and esters, clomeprop (N.13.11), clopyralid (N.13.12) and itssalts and esters, dicamba (N.13.13) and its salts and esters,dichlorprop (N.13.14) and its salts and esters, dichlorprop-P (N.13.15)and its salts and esters, fluroxypyr (N.13.16), fluroxypyr-butometyl(N.13.17), fluroxypyr-meptyl (N.13.18), halauxifen (N.13.) and its saltsand esters (CAS 943832-60-8); MCPA (N.13.) and its salts and esters,MCPA-thioethyl (N.13.19), MCPB (N.13.20) and its salts and esters,mecoprop (N.13.21) and its salts and esters, mecoprop-P (N.13.22) andits salts and esters, picloram (N.13.23) and its salts and esters,quinclorac (N.13.24), quinmerac (N.13.25), TBA (2,3,6) (N.13.26) and itssalts and esters, triclopyr (N.13.27) and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (N.13.28), benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate((N.13.29) CAS 1390661-72-9);

N.14 Auxin transport inhibitors: diflufenzopyr (N.14.1),diflufenzopyr-sodium (N.14.2), naptalam (N.14.3) and naptalam-sodium(N.14.4);

N.15 Other herbicides: bromobutide (N.15.1), chlorflurenol (N.15.2),chlorflurenol-methyl (N.15.3), cinmethylin (N.15.4), cumyluron (N.15.5),cyclopyrimorate ((N.15.6) CAS 499223-49-3) and its salts and esters,dalapon (N.15.7), dazomet (N.15.8), difenzoquat (N.15.9),difenzoquat-metilsulfate (N.15.10), dimethipin (N.15.11), DSMA(N.15.12), dymron (N.15.13), endothal (N.15.14) and its salts,etobenzanid (N.15.15), flurenol (N.15.16), flurenol-butyl (N.15.17),flurprimidol (N.15.18), fosamine (N.15.19), fosamine-ammonium (N.15.20),indanofan (N.15.21), maleic hydrazide (N.15.22), mefluidide (N.15.23),metam (N.15.24), methiozolin ((N.15.25) CAS 403640-27-7), methyl azide(N.15.26), methyl bromide (N.15.27), methyl-dymron (N.15.28), methyliodide (N.15.29), MSMA (N.15.30), oleic acid (N.15.31), oxaziclomefone(N.15.32), pelargonic acid (N.15.33), pyributicarb (N.15.34),quinoclamine (N.15.35), tridiphane (N.15.36);

O) Insecticides from Classes 0.1 to 0.29

O.1 Acetylcholine esterase (AChE) inhibitors: aldicarb (O.1.1),alanycarb (O.1.2), bendiocarb (O.1.3), benfuracarb (O.1.4), butocarboxim(O.1.5), butoxycarboxim (O.1.6), carbaryl (O.1.7), carbofuran (O.1.8),carbosulfan (O.1.9), ethiofencarb (O.1.10), fenobucarb (O.1.11),formetanate (O.1.12), furathiocarb (O.1.13), isoprocarb (O.1.14),methiocarb (O.1.15), methomyl (O.1.16), metolcarb (O.1.17), oxamyl(O.1.18), pirimicarb (O.1.19), propoxur (O.1.20), thiodicarb (O.1.21),thiofanox (O.1.22), trimethacarb (O.1.23), XMC (O.1.24), xylylcarb(O.1.25) and triazamate (O.1.26); acephate (O.1.27), azamethiphos(O.1.28), azinphos-ethyl (O.1.29), azinphosmethyl (O.1.30), cadusafos(O.1.31), chlorethoxyfos (O.1.32), chlorfenvinphos (O.1.33), chlormephos(O.1.34), chlorpyrifos (O.1.35), chlorpyrifosmethyl (O.1.36), coumaphos(O.1.37), cyanophos (O.1.38), demeton-S-methyl (O.1.39), diazinon(O.1.40), dichlorvos/DDVP (O.1.41), dicrotophos (O.1.42), dimethoate(O.1.43), dimethylvinphos (O.1.44), disulfoton (O.1.45), EPN (O.1.46),ethion (O.1.47), ethoprophos (O.1.48), famphur (O.1.49), fenamiphos(O.1.50), fenitrothion (O.1.51), fenthion (O.1.52), fosthiazate(O.1.53), heptenophos (O.1.54), imicyafos (O.1.55), isofenphos (O.1.56),isopropyl 0-(methoxyaminothio-phosphoryl) salicylate (O.1.57),isoxathion (O.1.58), malathion (O.1.59), mecarbam (O.1.60),methamidophos (O.1.61), methidathion (O.1.62), mevinphos (O.1.63),monocrotophos (O.1.64), naled (O.1.65), omethoate (O.1.66),oxydemeton-methyl (O.1.67), parathion (O.1.68), parathion-methyl(O.1.69), phenthoate (O.1.70), phorate (O.1.71), phosalone (O.1.72),phosmet (O.1.73), phosphamidon (O.1.74), phoxim (O.1.75),pirimiphos-methyl (O.1.76), profenofos (O.1.77), propetamphos (O.1.78),prothiofos (O.1.79), pyraclofos (O.1.80), pyridaphenthion (O.1.81),quinalphos (O.1.82), sulfotep (O.1.83), tebupirimfos (O.1.84), temephos(O.1.85), terbufos (O.1.86), tetrachlorvinphos (O.1.87), thiometon(O.1.88), triazophos (O.1.89), trichlorfon (O.1.90), vamidothion(O.1.91);

O.2 GABA-gated chloride channel antagonists: endosulfan (O.2.1),chlordane (O.2.2); ethiprole (O.2.3), fipronil (O.2.4), flufiprole(O.2.5), pyrafluprole (O.2.6), pyriprole (O.2.7);

O.3 Sodium channel modulators: acrinathrin (O.3.1), allethrin (O.3.2),d-cis-trans allethrin (O.3.3), d-trans allethrin (O.3.4), bifenthrin(O.3.5), bioallethrin (O.3.6), bioallethrin S-cylclopentenyl (O.3.7),bioresmethrin (O.3.8), cycloprothrin (O.3.9), cyfluthrin (O.3.10),beta-cyfluthrin (O.3.11), cyhalothrin (O.3.12), lambda-cyhalothrin(O.3.13), gamma-cyhalothrin (O.3.14), cypermethrin (O.3.15),alpha-cypermethrin (O.3.16), beta-cypermethrin (O.3.17),theta-cypermethrin (O.3.18), zeta-cypermethrin (O.3.19), cyphenothrin(O.3.20), deltamethrin (O.3.21), empenthrin (O.3.22), esfenvalerate(O.3.23), etofenprox (O.3.24), fenpropathrin (O.3.25), fenvalerate(O.3.26), flucythrinate (O.3.27), flumethrin (O.3.28), tau-fluvalinate(O.3.29), halfenprox (O.3.30), heptafluthrin (O.3.31), imiprothrin(O.3.32), meperfluthrin (O.3.33), metofluthrin (O.3.34), momfluorothrin(O.3.35), permethrin (O.3.36), phenothrin (O.3.37), prallethrin(O.3.38), profluthrin (O.3.39), pyrethrin (pyrethrum) (O.3.40),resmethrin (O.3.41), silafluofen (O.3.42), tefluthrin (O.3.43),tetramethylfluthrin (O.3.44), tetramethrin (O.3.45), tralomethrin(O.3.46) and transfluthrin (O.3.47); DDT (O.3.48), methoxychlor(O.3.49);

O.4 Nicotinic acetylcholine receptor agonists (nAChR): acetamiprid(O.4.1), clothianidin (O.4.2), cycloxaprid (O.4.3), dinotefuran (O.4.4),imidacloprid (O.4.5), nitenpyram (O.4.6), thiacloprid (O.4.7),thiamethoxam (O.4.8);(2E)-1-[(6-chloropyridin-3-yl)methyl]-N′-nitro-2-pentylidenehydrazinecarboximidamide(O.4.9);1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine(O.4.10); nicotine (O.4.11);

O.5 Nicotinic acetylcholine receptor allosteric activators: spinosad(O.5.1), spinetoram (O.5.2);

O.6 Chloride channel activators: abamectin (O.6.1), emamectin benzoate(O.6.2), ivermectin (O.6.3), lepimectin (O.6.4), milbemectin (O.6.5);

O.7 Juvenile hormone mimics: hydroprene (O.7.1), kinoprene (O.7.2),methoprene (O.7.3); fenoxycarb (O.7.4), pyriproxyfen (O.7.5);

O.8 miscellaneous non-specific (multi-site) inhibitors: methyl bromide(O.8.1) and other alkyl halides; chloropicrin (O.8.2), sulfuryl fluoride(O.8.3), borax (O.8.4), tartar emetic (O.8.5);

O.9 Selective homopteran feeding blockers: pymetrozine (O.9.1),flonicamid (O.9.2);

O.10 Mite growth inhibitors: clofentezine (O.10.1), hexythiazox(O.10.2), diflovidazin (O.10.3); etoxazole (O.10.4);

O.11 Microbial disruptors of insect midgut membranes: the Bt cropproteins: Cry1Ab, Cry1Ac, Cry1Fa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb,Cry34/35Ab1;

O.12 Inhibitors of mitochondrial ATP synthase: diafenthiuron (O.12.1);azocyclotin (O.12.2), cyhexatin (O.12.3), fenbutatin oxide (O.12.4),propargite (O.12.5), tetradifon (O.12.6);

O.13 Uncouplers of oxidative phosphorylation via disruption of theproton gradient: chlorfenapyr (O.13.1), DNOC (O.13.2), sulfluramid(O.13.3);

O.14 Nicotinic acetylcholine receptor (nAChR) channel blockers:bensultap (O.14.1), cartap hydrochloride (O.14.2), thiocyclam (O.14.3),thiosultap sodium (O.14.4);

O.15 Inhibitors of the chitin biosynthesis type 0: bistrifluron(O.15.1), chlorfluazuron (O.15.2), diflubenzuron (O.15.3), flucycloxuron(O.15.4), flufenoxuron (O.15.5), hexaflumuron (O.15.6), lufenuron(O.15.7), novaluron (O.15.8), noviflumuron (O.15.9), teflubenzuron(O.15.10), triflumuron (O.15.11);

O.16 Inhibitors of the chitin biosynthesis type 1: buprofezin (O.16.1);

O.17 Moulting disruptors: cyromazine (O.17.1);

O.18 Ecdyson receptor agonists: methoxyfenozide (O.18.1), tebufenozide(O.18.2), halofenozide (O.18.3), fufenozide (O.18.4), chromafenozide(O.18.5);

O.19 Octopamin receptor agonists: amitraz (O.19.1);

O.20 Mitochondrial complex III electron transport inhibitors:hydramethylnon (O.20.1), acequinocyl (O.20.2), fluacrypyrim (O.20.3);

O.21 Mitochondrial complex I electron transport inhibitors: fenazaquin(O.21.1), fenpyroximate (O.21.2), pyrimidifen (O.21.3), pyridaben(O.21.4), tebufenpyrad (O.21.5), tolfenpyrad (O.21.6); rotenone(O.21.7);

O.22 Voltage-dependent sodium channel blockers: indoxacarb (O.22.1),metaflumizone(O.22.2),2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide(O.22.3),N-(3-chloro-2-methylphenyl)-2-[(4-chlorophenyl)-[4-[methyl(methylsulfonyl)amino]phenyl]methylene]-hydrazinecarboxamide(O.22.4);

O.23 Inhibitors of the of acetyl CoA carboxylase: spirodiclofen(O.23.1), spiromesifen (O.23.2), spirotetramat (O.23.3);

O.24 Mitochondrial complex IV electron transport inhibitors: aluminiumphosphide (O.24.1), calcium phosphide (O.24.2), phosphine (O.24.3), zincphosphide (O.24.4), cyanide (O.24.5);

O.25 Mitochondrial complex II electron transport inhibitors:cyenopyrafen (O.25.1), cyflumetofen (O.25.2);

O.26 Ryanodine receptor-modulators: flubendiamide (O.26.1),chlorantraniliprole (O.26.2), cyantraniliprole (O.26.3), cyclaniliprole(O.26.4), tetraniliprole (O.26.5);(R)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide(O.26.6),(S)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide(O.26.7),methyl-2-[3,5-dibromo-2-({[3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl]carbonyl}-amino)benzoyl]-1,2-dimethylhydrazinecarboxylate(O.26.8);N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.9);N-[4-chloro-2-[(diethyl-ambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.10);N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.11);N-[4,6-dichloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.12);N-[4,6-dibromo-2-[(diethyl-ambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazoe-3-carboxamide(O.26.13);N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(O.26.14);3-chloro-1-(3-chloro-2-pyridinyl)-N-[2,4-dichloro-6-[[(1-cyano-1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide(O.26.15);3-bromo-N-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-1-(3,5-dichloro-2-pyridyl)-1H-pyrazole-5-carboxamide(O.26.16);N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-pyrazole-5-carboxamide(O.26.17); cyhalodiamide (O.26.18);

O.27. insecticidal active compounds of unknown or uncertain mode ofaction: afidopyropen (O.27.1), afoxolaner (O.27.2), azadirachtin(O.27.3), amidoflumet (O.27.4), benzoximate (O.27.5), bifenazate(O.27.6), broflanilide (O.27.7), bromopropylate (O.27.8), chinomethionat(O.27.9), cryolite (O.27.10), dicloromezotiaz (O.27.11), dicofol(O.27.12), flufenerim (O.27.13), flometoquin (O.27.14), fluensulfone(O.27.15), fluhexafon (O.27.16), fluopyram (O.27.17), flupyradifurone(O.27.18), fluralaner (O.27.19), metoxadiazone (O.27.20), piperonylbutoxide (O.27.21), pyflubumide (O.27.22), pyridalyl (O.27.23),pyrifluquinazon (O.27.24), sulfoxaflor (O.27.25), tioxazafen (O.27.26),triflumezopyrim (O.27.27),11-(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1,4-dioxa-9-azadispiro[4.2.4.2]-tetradec-11-en-10-one(O.27.28),3-(4′-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1-azaspiro[4.5]dec-3-en-2-one(O.27.28),1-[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine(O.27.29),(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.31);(E/Z)—N-[1-[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.32);(E/Z)-2,2,2-trifluoro-N-[1-[(6-fluoro-3-pyridyl)methyl]-2-pyridylidene]acetamide(O.27.33);(E/Z)—N-[1-[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.34);(E/Z)—N-[1-[1-(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.35);(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide(O.27.36);(E/Z)-2-chloro-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide(O.27.37);(E/Z)—N-[1-[(2-chloropyrimidin-5-yl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.38);(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,3,3,3-pentafluoro-propanamide(O.27.39);N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-thioacetamide(O.27.40);N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-N′-isopropyl-acetamidine(O.27.41); fluazaindolizine (O.27.42);4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-N-(1-oxothietan-3-yl)benzamide(O.27.43); fluxametamide (O.27.44);5-[3-[2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy]propoxy]-1H-pyrazole(O.27.45);3-(benzoylmethylamino)-N-[2-bromo-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]-6-(trifluoromethyl)phenyl]-2-fluoro-benzamide(O.27.46);3-(benzoylmethylamino)-2-fluoro-N-[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]-benzamide(O.27.47);N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.48);N-[3-[[[2-bromo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]-2-fluorophenyl]-4-fluoro-N-methyl-benzamide(O.27.49);4-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.50);3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.51);2-chloro-N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-3-pyridinecarboxamide(O.27.52);4-cyano-N-[2-cyano-5-[[2,6-dibromo-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.53);4-cyano-3-[(4-cyano-2-methyl-benzoyl)amino]-N-[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]-2-fluoro-benzamide(O.27.54);N-[5-[[2-chloro-6-cyano-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]-phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.55);N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.56);N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.57);4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)-propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.58);4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.59);N-[5-[[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.60); 2-(1,3-dioxan-2-yl)-6-[2-(3-pyridinyl)-5-thiazolyl]-pyridine;2-[6-[2-(5-fluoro-3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine(O.27.61); 2-[6-[2-(3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine(O.27.62);N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide(O.27.63);N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide(O.27.64);N-ethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.65);N-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.66);N,2-dimethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.67);N-ethyl-2-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.68);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-2-methyl-3-methylthio-propanamide(O.2769.);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N,2-dimethyl-3-methylthio-propanamide(O.27.70);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-methyl-3-methylthio-propanamide(O.27.71);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-3-methylthio-propanamide(O.27.72);1-[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo[1,2-a]pyridine(O.27.73);1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridin-5-ol(O.27.74);1-isopropyl-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.75);1-(1,2-dimethylpropyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.76);N,5-dimethyl-N-pyridazin-4-yl-1-(2,2,2-trifluoro-1-methyl-ethyl)pyrazole-4-carboxamide(O.27.77);1-[1-(1-cyanocyclopropyl)ethyl]-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.78);N-ethyl-1-(2-fluoro-1-methyl-propyl)-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.79);1-(1,2-dimethylpropyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.80);1-[1-(1-cyanocyclopropyl)ethyl]-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.81);N-methyl-1-(2-fluoro-1-methyl-propyl]-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.82);1-(4,4-difluorocyclohexyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.83);1-(4,4-difluorocyclohexyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.84), N-(1-methylethyl)-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.85); N-cyclopropyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.86); N-cyclohexyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.87);2-(3-pyridinyl)-N-(2,2,2-trifluoroethyl)-2H-indazole-4-carboxamide(O.27.88);2-(3-pyridinyl)-N-[(tetrahydro-2-furanyl)methyl]-2H-indazole-5-carboxamide(O.27.89); methyl2-[[2-(3-pyridinyl)-2H-indazol-5-yl]carbonyl]hydrazinecarboxylate(O.27.90);N-[(2,2-difluorocyclopropyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-carboxamide(O.27.91);N-(2,2-difluoropropyl)-2-(3-pyridinyl)-2H-indazole-5-carboxamide(O.27.92);2-(3-pyridinyl)-N-(2-pyrimidinylmethyl)-2H-indazole-5-carboxamide(O.27.93);N-[(5-methyl-2-pyrazinyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-carboxamide(O.27.94),N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfanyl)-propanamide(O.27.95);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfinyl)propanamide(O.27.96);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-di-fluorocyclopropyl)methylsulfanyl]-N-ethyl-propanamide(O.27.97);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-difluorocyclopropyl)methylsulfinyl]-N-ethyl-propanamide(O.27.98); sarolaner (O.27.99), lotilaner (O.27.100);

in a weight ratio of from 100:1 to 1:100.

The invention also relates to a method for controlling phytopathogenicharmful fungi using mixtures comprising as component 1) of at least onecompound of the formula I and comprising as component 2) at least onecompound II in a weight ratio of from 100:1 to 1:100; to the use ofmixtures comprising compounds I and compounds II for controllingphytopathogenic harmful fungi; to agrochemical compositions comprisingthese mixtures; and to agrochemical compositions further comprisingseed.

Practical agricultural experience has shown that the repeated andexclusive application of an individual active compound in the control ofharmful fungi leads in many cases to a rapid selection of those fungusstrains which have developed natural or adapted resistance against theactive compound in question. Effective control of these fungi with theactive compound in question is then no longer possible.

To reduce the risk of the selection of resistant fungus strains,mixtures of different active compounds are conventionally employed forcontrolling harmful fungi. By combining active compounds havingdifferent mechanisms of action, it is possible to ensure successfulcontrol over a relatively long period of time.

It is an object of the present invention to provide, with a view toeffective resistance management and effective control of phytopathogenicharmful fungi, at application rates which are as low as possible,compositions which, at a reduced total amount of active compoundsapplied, have improved activity against the harmful fungi (synergisticmixtures) and a broadened activity spectrum, in particular for certainindications.

We have accordingly found that this object is achieved by thecompositions, defined herein, comprising at least one compound I and atleast one compound II.

Moreover, we have found that simultaneous, that is joint or separate,application of a compound I and a compound II or successive applicationof a compound I and of compound II allows better control of harmfulfungi than is possible with the individual compounds alone (synergisticmixtures). Compounds I and/or the compounds II can be present indifferent crystal modifications, which may differ in biologicalactivity.

The term “compounds I” refers to compounds of formula I.

In the definitions of the variables given above, collective terms areused which are generally representative for the substituents inquestion. The term “C_(n)-C_(m)” indicates the number of carbon atomspossible in each case in the substituent or substituent moiety inquestion.

The term “halogen” refers to fluorine, chlorine, bromine and iodine.

The term “C₁-C₆-alkyl” refers to a straight-chained or branchedsaturated hydrocarbon group having 1 to 6 carbon atoms, for examplemethyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl,2-methylpropyl, and 1,1-dimethylethyl.

The term “C₂-C₆-alkenyl” refers to a straight-chain or branchedunsaturated hydrocarbon radical having 2 to 6 carbon atoms and a doublebond in any position, such as ethenyl, 1-propenyl, 2-propenyl (allyl),1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl,2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl.

The term “C₂-C₆-alkynyl” refers to a straight-chain or branchedunsaturated hydrocarbon radical having 2 to 6 carbon atoms andcontaining at least one triple bond, such as ethynyl, 1-propynyl,2-propynyl (propargyl), 1-butynyl, 2-butynyl, 3-butynyl,1-methyl-2-propynyl.

The term “C₁-C₆-haloalkyl” refers to a straight-chained or branchedalkyl group having 1 to 6 carbon atoms (as defined above), wherein someor all of the hydrogen atoms in these groups may be replaced by halogenatoms as mentioned above, for example chloromethyl, bromomethyl,dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl,trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl,chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl,2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl,2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl,2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl,2-fluoropropyl, 3-fluoropropyl, 2,2-difluoropropyl, 2,3-difluoropropyl,2-chloropropyl, 3-chloropropyl, 2,3-dichloropropyl, 2-bromopropyl,3-bromopropyl, 3,3,3-trifluoropropyl, 3,3,3-trichloropropyl, CH₂—C₂F₅,CF₂—C₂F₅, CF(CF₃)₂, 1-(fluoromethyl)-2-fluoroethyl,1-(chloromethyl)-2-chloroethyl, 1-(bromomethyl)-2-bromoethyl,4-fluorobutyl, 4-chlorobutyl, 4-bromobutyl or nonafluorobutyl.

The term “C₁-C₆-alkoxy” refers to a straight-chain or branched alkylgroup having 1 to 6 carbon atoms (as defined above) which is bonded viaan oxygen, at any position in the alkyl group, for example methoxy,ethoxy, n-propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy,2-methylpropoxy or 1,1-dimethylethoxy.

The term “C₃-C₈-cycloalkyl” refers to monocyclic saturated hydrocarbonradicals having 3 to 8 carbon ring members such as cyclopropyl (C₃H₅),cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.

The term “aliphatic” refers to compounds or radicals composed of carbonand hydrogen and which are non-aromatic compounds. An “alicyclic”compound or radical is an organic compound that is both aliphatic andcyclic. They contain one or more all-carbon rings which may be eithersaturated or unsaturated, but do not have aromatic character.

The term “cyclic group” refers to a radical which is an alicyclic ringor an aromatic ring, such as, for example, phenyl or heteroaryl.

The term “and wherein any of the aliphatic or cyclic groups areunsubstituted or substituted with . . . ” refers to aliphatic groups,cyclic groups and groups, which contain an aliphatic and a cyclic moietyin one group, such as in, for example, C₃-C₅-cycloalkyl-C₁-C₄-alkyl;therefore a group which contains an aliphatic and a cyclic moiety bothof these moieties may be substituted or unsubstituted independently ofeach other.

The term “phenyl” refers to an aromatic ring systems including sixcarbon atoms (commonly referred to as benzene ring).

Agriculturally acceptable salts of the active compounds I, and IIIencompass especially the salts of those cations or the acid additionsalts of those acids whose cations and anions, respectively, have noadverse effect on the fungicidal action of the active compounds.Suitable cations are thus in particular the ions of the alkali metals,preferably sodium and potassium, of the alkaline earth metals,preferably calcium, magnesium and barium, of the transition metals,preferably manganese, copper, zinc and iron, and also the ammonium ionwhich, if desired, may carry 1 to 4 C₁-C₄-alkyl substituents and/or onephenyl or benzyl substituent, preferably diisopropylammonium,tetramethylammonium, tetrabutylammonium, trimethylbenzylammonium,furthermore phosphonium ions, sulfonium ions, preferablytri(C₁-C₄-alkyl)sulfonium, and sulfoxonium ions, preferablytri(C₁-C₄-alkyl)sulfoxonium. Anions of useful acid addition salts areprimarily chloride, bromide, fluoride, hydrogensulfate, sulfate,dihydrogenphosphate, hydrogen-phosphate, phosphate, nitrate,bicarbonate, carbonate, hexafluorosilicate, hexafluorophosphate,benzoate, and the anions of C₁-C₄-alkanoic acids, preferably formate,acetate, propionate and butyrate. They can be formed by reacting acompound I with an acid of the corresponding anion, preferably ofhydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid ornitric acid.

The scope of the present invention includes mixtures of the (R)- and(S)-isomers and the racemates of compounds I and/or II and/or III havingone or more chiral centers. As a result of hindered rotation ofasymmetrically substituted groups, atrope isomers of active compounds 1and/or and/or III may be present. They also form part of the subjectmatter of the invention.

The active substances referred to as compounds II or III, theirpreparation and their activity e. g. against harmful fungi is known(cf.: http://www.alanwood.net/pesticides/); these substances arecommercially available. The compounds described by IUPAC nomenclature,their preparation and their pesticidal activity are also known (cf. Can.J. Plant Sci. 48(6), 587-94, 1968; EP-A 141 317; EP-A 152 031; EP-A 226917; EP-A 243 970; EP-A 256 503; EP-A 428 941; EP-A 532 022; EP-A 1 028125; EP-A 1 035 122; EP-A 1 201 648; EP-A 1 122 244, JP 2002316902; DE19650197; DE 10021412; DE 102005009458; U.S. Pat. Nos. 3,296,272;3,325,503; WO 98/46608; WO 99/14187; WO 99/24413; WO 99/27783; WO00/29404; WO 00/46148; WO 00/65913; WO 01/54501; WO 01/56358; WO02/22583; WO 02/40431; WO 03/10149; WO 03/11853; WO 03/14103; WO03/16286; WO 03/53145; WO 03/61388; WO 03/66609; WO 03/74491; WO04/49804; WO 04/83193; WO 05/120234; WO 05/123689; WO 05/123690; WO05/63721; WO 05/87772; WO 05/87773; WO 06/15866; WO 06/87325; WO06/87343; WO 07/82098; WO 07/90624, WO 10/139271, WO 11/028657, WO12/168188, WO 07/006670, WO 11/77514; WO 13/047749, WO 10/069882, WO13/047441, WO 03/16303, WO 09/90181, WO 13/007767, WO 13/010862, WO13/127704, WO 13/024009, WO 13/24010, WO 13/047441, WO 13/162072, WO13/092224, WO 11/135833, CN 1907024, CN 1456054, CN 103387541, CN1309897, WO 12/84812, CN 1907024, WO 09094442, WO 14/60177, WO13/116251, WO 08/013622, WO 15/65922, WO 94/01546, EP 2865265, WO07/129454, WO 12/165511, WO 11/081174, WO 13/47441).

Compounds of the formula I and their preparation and their use asfungicidally active compounds have been described in WO2015/185485 A1and in the unpublished International applications WO 2017/076742 A1, WO2017/081311 A1, WO 2017/085100 A1, WO 2017/093019 A1 and WO 2017/178245A1.

Compounds of the formula I, wherein W contains a —C(═S)— group, can beprepared by reacting corresponding carboxamides with a sulfonationreagent, preferably Lawessons reagent(2,4-Bis-(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetan-2,4-disulfid), inan organic solvent, preferably at temperatures between 20° C. and 150°C., preferably at 110° C., as previously described (see for exampleJournal of Organic Chemistry, 2008, 73, 9102 or European Journal ofOrganic Chemistry, 2015, 30, 6687).

In one embodiment the present invention relates to mixtures comprisingas component 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof, wherein:

-   W is —(C═O)—NR²-#, —(C═S)—NR²-#, —NR²—(C═O)-# or —NR²—(C═S)-#;    wherein # denotes the position, which is attached to the group R¹;-   R¹ is alkoxyimino-C₁-C₄-alkyl;-   R² is hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,    C₁-C₆-alkoxy, C₃-C₈-cycloalkyl, C₃-C₅-cycloalkenyl, and    C₃-C₅-cycloalkyl-C₁-C₄-alkyl; and wherein any of the aliphatic or    cyclic groups are unsubstituted or substituted with 1, 2, 3 or up to    the maximum possible number of identical or different radicals    selected from the group consisting of halogen, hydroxy, oxo, cyano,    C₁-C₆-alkyl, C₁-C₆-alkoxy and C₃-C₈-cycloalkyl;-   m is 0 or 1;-   R³, R⁴ independently of each other are selected from the group    consisting of hydrogen, fluorine and methyl;-   or R³ and R⁴ together with the carbon atom to which they are bound    form a cyclopropyl ring.

In one embodiment the present invention relates to mixtures comprisingas component 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof, wherein:

-   W is —NR²—(C═O)-# or —NR²—(C═S)-#; wherein # denotes the position,    which is attached to the group R¹;-   R¹ is C₁—C-alkyl or C₃-C₈-cycloalkyl;-   R² is C₂-C₆-alkenyl or C₂-C₆-alkynyl; and wherein any of the    aliphatic or cyclic groups are unsubstituted or substituted with 1,    2, 3 or up to the maximum possible number of identical or different    radicals selected from the group consisting of halogen, hydroxy,    oxo, cyano, C₁-C₆-alkyl, C₁-C₆-alkoxy and C₃-C₈-cycloalkyl;-   m is 0 or 1;-   R³, R⁴ independently of each other are selected from the group    consisting of hydrogen, fluorine and methyl;-   or R³ and R⁴ together with the carbon atom to which they are bound    form a cyclopropyl ring.

In one embodiment the present invention relates to mixtures comprisingas component 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof, wherein:

-   W is —NR²—(C═O)-# or —NR²—(C═S)-#; wherein # denotes the position,    which is attached to the group R¹;-   R¹ and R² together with the nitrogen atom to which they are bound    form a saturated or partially unsaturated mono- or bicyclic 3- to    7-membered heterocycle, wherein the heterocycle includes beside one    nitrogen atom and one or more carbon atoms no further heteroatom or    1, 2 or 3 further heteroatoms independently selected from N, O and S    as ring member atoms; and wherein one or two CH₂ groups of the    heterocycle may be replaced by one or two groups independently    selected from the group of C(═O) and C(═S); and wherein the    heterocycle is unsubstituted or carries 1, 2, 3, 4 or up to the    maximum possible number of identical or different radicals selected    from the group consisting of halogen, cyano, C1-C₆-alkyl,    C₁-C₆-haloalkyl, C₁-C₆-alkoxy,-   m is 1;-   R³, R⁴ independently of each other are selected from the group    consisting of hydrogen, fluorine and methyl;-   or R³ and R⁴ together with the carbon atom to which they are bound    form a cyclopropyl ring.

In one embodiment the present invention relates to mixtures comprisingas component 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof, wherein:

-   W is —(C═O)—NR²-# or —(C═S)—NR²-#; wherein # denotes the position,    which is attached to the group R¹;-   m is 0;-   R¹ is C₁-C₆-alkyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl,    C₂-C₆-alkenyl, C₂-C₆-alkynyl or phenyl; wherein the phenyl ring is    unsubstituted or substituted with 1, 2, 3 or up to the maximum    possible number of identical or different radicals selected from the    group consisting of halogen;-   R² is hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,    C₁-C₆-alkoxy, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, and    C₃-C₅-cycloalkyl-C₁-C₄-alkyl; and wherein any of the aliphatic or    cyclic groups are unsubstituted or substituted with 1, 2, 3 or up to    the maximum possible number of identical or different radicals    selected from the group consisting of halogen, hydroxy, oxo, cyano,    C₁-C₆-alkyl, C₁-C₆-alkoxy and C₃-C₈-cycloalkyl.

In one embodiment the present invention relates to mixtures comprisingas component 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof, wherein:

-   W is —(C═O)—NR²-# or —(C═S)—NR²-#; wherein # denotes the position,    which is attached to the group R¹;-   m is 0;-   R¹ is methyl, ethyl, n-propyl, iso-propyl, cyclopropyl or    2-fluorophenyl;-   R² is hydrogen.

Particularly preferred active compounds I are selected from the groupconsisting of compounds I.A to I.N:

I.A: N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide I.B:N-[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamideI.C:N-[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamideI.D:N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamideI.E:N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamideI.F:2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]acetamideI.G:N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]acetamideI.H:N-[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide I.J:N-[(Z)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide I.K:N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamideI.L4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one I.MN-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamideI.N5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one

In one aspect of the invention active compounds I are selected from thegroup of compounds consisting of I.B, I.C, I.D, I.F, I.G, I.H, I.K, I.Land I.N.

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from inhibitors of complex III at Q_(o)site in group A), more preferably selected from compounds (A.1.1),(A.1.4), (A.1.8), (A.1.9), (A.1.10), (A.1.11), (A.1.12), (A.1.13),(A.1.14), (A.1.17), (A.1.21), (A.1.21a), (A.1.24), (A.1.25), (A.1.26),(A.1.27), (A.1.30), (A.1.31), (A.1.32), (A.1.34) and (A.1.35);particularly selected from (A.1.1), (A.1.8), (A.1.9), (A.1.10),(A.1.11), (A.1.13), (A.1.14), (A.1.17), (A.1.25) and (A.1.34).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from inhibitors of complex III at Q_(i)site in group A), more preferably selected from compounds (A.2.1),(A.2.3), (A.2.4), (A.2.5) and (A.2.6); particularly selected from(A.2.4) and (A.2.6).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from inhibitors of complex II in group A),more preferably selected from compounds (A.3.2), (A.3.3), (A.3.4),(A.3.7), (A.3.9), (A.3.11), (A.3.12), (A.3.15), (A.3.16), (A.3.17),(A.3.18), (A.3.19), (A.3.20), (A.3.21), (A.3.22), (A.3.23), (A.3.24),(A.3.25), (A.3.26), (A.3.27), (A.3.28), (A.3.29), (A.3.31), (A.3.32),(A.3.33), (A.3.34), (A.3.35), (A.3.36), (A.3.37), (A.3.38) and (A.3.39);particularly selected from (A.3.2), (A.3.3), (A.3.4), (A.3.7), (A.3.9),(A.3.17), (A.3.24), (A.3.28), (A.3.29), (A.3.31), (A.3.32), (A.3.33),(A.3.34), (A.3.35), (A.3.36), (A.3.37), (A.3.38) and (A.3.39).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from other respiration inhibitors in groupA), more preferably selected from compounds (A.4.5) and (A.4.11).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from C14 demethylase inhibitors in groupB), more preferably selected from compounds (B.1.4), (B.1.5), (B.1.8),(B.1.10), (B.1.11), (B.1.12), (B.1.13), (B.1.17), (B.1.18), (B.1.21),(B.1.22), (B.1.23), (B.1.25), (B.1.26), (B.1.29), (B.1.33), (B.1.34),(B.1.37), (B.1.38), (B.1.43) and (B.1.46); particularly selected from(B.1.4), (B.1.5), (B.1.8), (B.1.17), (B.1.22), (B.1.23), (B.1.25),(B.1.29), and (B.1.38).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from Delta14-reductase inhibitors in groupB), more preferably selected from compounds (B.2.4), (B.2.5), (B.2.6)and (B.2.8); in particular (B.2.4) and (B.2.6).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from phenylamides and acyl amino acidfungicides in group C), more preferably selected from compounds (C.1.1),(C.1.2), (C.1.4) and (C.1.5).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from other nucleic acid synthesisinhibitors in group C), more preferably selected from compounds (C.2.6),(C.2.7) and (C.2.8).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group D), more preferably selectedfrom compounds (D.1.1), (D.1.2), (D.1.5), (D.2.4), (D.2.6) and (D.2.7);particularly selected from (D.2.6) and (D.2.7).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group E), more preferably selectedfrom compounds (E.1.1), (E.1.3), (E.2.2) and (E.2.3); in particular(E.1.1).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group F), more preferably selectedfrom compounds (F.1.2), (F.1.4) and (F.1.5).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group G), more preferably selectedfrom compounds (G.3.1), (G.3.3), (G.3.6), (G.5.1), (G.5.2), (G.5.3),(G.5.4), (G.5.5), G.5.6), G.5.7), (G.5.8), (G.5.9), (G.5.10) and(G.5.11).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group H), more preferably selectedfrom compounds (H.1.5), (H.1.7), (H.2.2), (H.2.3), (H.2.5), (H.2.7),(H.2.8), (H.3.2), (H.3.4), (H.3.5), (H.4.9) and (H.4.10); particularlyselected from (H.1.5), (H.1.7), (H.2.2), (H.3.2) and (H.3.5).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group 1), more preferably selectedfrom compounds (I.2.2) and (I.2.5).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group J), more preferably selectedfrom compounds (J.1.2), (J.1.5), (J.1.8), (J.1.11) and (J.1.12).

Preference is also given to mixtures comprising as component 2) at leastone active compound selected from group K), more preferably selectedfrom compounds (K.1.3), (K.1.29), (K.1.30), (K.1.31), (K.1.32),(K.1.41), (K.1.42), (K.1.44), (K.1.45), (K.1.47), (K.1.49) and (K.1.54);particularly selected from (K.1.3), (K.1.29), (K.1.30), (K.1.31),(K.1.32), (K.1.42), (K.1.53) and (K.1.54).

Particularly preferred are the following binary mixtures A-1 to A-739listed in Table A, wherein compounds I (component 1, a group representedby the expression “(1)” consisting of compounds I.A, I.B, I.C, I.D, I.E,I.F, I.G, I.H, I.J, I.K, I.L, I.M and I.N) and one pesticide II selectedfrom the groups A) to O) as defined herein (component 2, for example,(A.1.1) or azoxystrobin, in mixture A-1).

TABLE A A-1: (I) + (A.1.1), A-2: (I) + (A.1.2), A-3: (I) + (A.1.3), A-4:(I) + (A.1.4), A-5: (I) + (A.1.5), A-6: (I) + (A.1.6), A-7: (I) +(A.1.7), A-8: (I) + (A.1.8), A-9: (I) + (A.1.9), A-10: (I) + (A.1.10),A-11: (I) + (A.1.11), A-12: (I) + (A.1.12), A-13: (I) + (A.1.13), A-14:(I) + (A.1.14), A-15: (I) + (A.1.15), A-16: (I) + (A.1.16), A-17: (I) +(A.1.17), A-18: (I) + (A.1.18), A-19: (I) + (A.1.19), A-20: (I) +(A.1.20), A-21: (I) + (A.1.21), A-22: (I) + (A.1.22), A-23: (I) +(A.1.23), A-24: (I) + (A.1.24), A-25: (I) + (A.1.25), A-26: (I) +(A.1.26), A-27: (I) + (A.1.27), A-28: (I) + (A.1.30), A-29: (I) +(A.1.31), A-30: (I) + (A.1.32), A-31: (I) + (A.2.1), A-32: (I) +(A.2.2), A-33: (I) + (A.2.3), A-34: (I) + (A.2.4), A-35: (I) + (A.2.6),A-36: (I) + (A.2.7), A-37: (I) + (A.2.8), A-38: (I) + (A.3.1), A-39:(I) + (A.3.2), A-40: (I) + (A.3.3), A-41: (I) + (A.3.4), A-42: (I) +(A.3.5), A-43: (I) + (A.3.6), A-44: (I) + (A.3.7), A-45: (I) + (A.3.8),A-46: (I) + (A.3.9), A-47: (I) + (A.3.10), A-48: (I) + (A.3.11), A-49:(I) + (A.3.12), A-50: (I) + (A.3.13), A-51: (I) + (A.3.14), A-52: (I) +(A.3.15), A-53: (I) + (A.3.16), A-54: (I) + (A.3.17), A-55: (I) +(A.3.18), A-56: (I) + (A.3.19), A-57: (I) + (A.3.20), A-58: (I) +(A.3.21), A-59: (I) + (A.3.22), A-60: (I) + (A.3.23), A-61: (I) +(A.3.24), A-62: (I) + (A.3.25), A-63: (I) + (A.3.26), A-64: (I) +(A.3.27), A-65: (I) + (A.3.28), A-66: (I) + (A.3.29), A-67: (I) +(A.3.30), A-68: (I) + (A.3.31), A-69: (I) + (A.3.32), A-70: (I) +(A.3.33), A-71: (I) + (A.3.34), A-72: (I) + (A.3.35), A-73: (I) +(A.3.36), A-74: (I) + (A.3.37), A-75: (I) + (A.3.38), A-76: (I) +(A.3.39), A-77: (I) + (A.4.1), A-78: (I) + (A.4.2), A-79: (I) + (A.4.3),A-80: (I) + (A.4.4), A-81: (I) + (A.4.5), A-82: (I) + (A.4.6), A-83:(I) + (A.4.7), A-84: (I) + (A.4.8), A-85: (I) + (A.4.9), A-86: (I) +(A.4.10), A-87: (I) + (A.4.11), A-88: (I) + (A.4.12), A-89: (I) +(B.1.1), A-90: (I) + (B.1.2), A-91: (I) + (B.1.3), A-92: (I) + (B.1.4),A-93: (I) + (B.1.5), A-94: (I) + (B.1.6), A-95: (I) + (B.1.7), A-96:(I) + (B.1.8), A-97: (I) + (B.1.9), A-98: (I) + (B.1.10), A-99: (I) +(B.1.11), A-100: (I) + (B.1.12), A-101: (I) + (B.1.13), A-102: (I) +(B.1.14), A-103: (I) + (B.1.15), A-104: (I) + (B.1.16), A-105: (I) +(B.1.17), A- 106: (I) + (B.1.18), A-107: (I) + (B.1.19), A-108: (I) +(B.1.20), A-109: (I) + (B. 1.21), A-110: (I) + (B.1.22), A-111: (I) +(B.1.23), A-112: (I) + (B.1.24), A-113: (I) + (B.1.25), A-114: (I) +(B.1.26), A- 115: (I) + (B.1.27), A-116: (I) + (B.1.28), A-117: (I) +(B.1.29), A-118: (I) + (B.1.30), A-119: (I) + (B.1.34), A-120: (I) +(B.1.37), A-121: (I) + (B.1.38), A-122: (I) + (B.1.43), A-123: (I) +(B.1.44), A- 124: (I) + (B.1.45), A-125: (I) + (B.1.46), A-126: (I) +(B.1.47), A-127: (I) + (B.1.48), A-128: (I) + (B.1.49), A-129: (I) +(B.1.50), A-130: (I) + (B.1.51), A-131: (I) + (B.2.1), A-132: (I) +(B.2.2), A- 133: (I) + (B.2.3), A-141: (I) + (B.2.4), A-135: (I) +(B.2.5), A-136: (I) + (B.2.6), A-137: (I) + (B.2.7), A- 138: (I) +(B.2.8), A-139: (I) + (B.3.1), A-140: (I) + (C.1.1), A-141: (I) +(C.1.2), A-142: (I) + (C. 1.3), A- 143: (I) + (C.1.4), A-144: (I) +(C.1.5), A-145: (I) + (C.1.6), A-146: (I) + (C.1.7), A-147: (I) +(C.2.1), A- 148: (I) + (C.2.2), A-149: (I) + (C.2.3), A-150: (I) +(C.2.4), A-151: (I) + (C.2.5), A-152: (I) + (C.2.6), A- 153: (I) +(C.2.7), A-154: (I) + (D.1.1), A-155: (I) + (D.1.2), A-156: (I) +(D.1.3), A-157: (I) + (D. 1.4), A- 158: (I) + (D.1.5), A-159: (I) +(D.1.6), A-160: (I) + (D.2.1), A-161: (I) + (D.2.2), A-162: (I) +(D.2.3), A- 163: (I) + (D.2.4), A-164: (I) + (D.2.5), A-165: (I) +(D.2.6), A-166: (I) + (D.2.7), A-167: (I) + (E. 1.1), A- 168: (I) +(E.1.2), A-169: (I) + (E.1.3), A-170: (I) + (E.2.1), A-171: (I) +(E.2.2), A-172: (I) + (E.2.3), A- 173: (I) + (E.2.4), A-174: (I) +(E.2.5), A-175: (I) + (E.2.6), A-176: (I) + (E.2.7), A-177: (I) +(E.2.8), A- 178: (I) + (F.1.1), A-179: (I) + (F.1.2), A-180: (I) +(F.1.3), A-181: (I) + (F.1.4), A-182: (I) + (F.1.5), A- 183: (I) +(F.1.6), A-184: (I) + (F.2.1), A-185: (I) + (G.1.1), A-186: (I) +(G.1.2), A-187: (I) + (G.1.3), A- 188: (I) + (G.1.4), A-189: (I) +(G.2.1), A-190: (I) + (G.2.2), A-191: (I) + (G.2.3), A-192: (I) +(G.2.4), A- 193: (I) + (G.2.5), A-194: (I) + (G.2.6), A-195: (I) +(G.2.7), A-196: (I) + (G.3.1), A-197: (I) + (G.3.2), A- 198: (I) +(G.3.3), A-199: (I) + (G.3.4), A-200: (I) + (G.3.5), A-201: (I) +(G.3.6), A-202: (I) + (G.3.7), A- 203: (I) + (G.3.8), A-204: (I) +(G.4.1), A-205: (I) + (G.5.1), A-206: (I) + (G.5.2), A-207: (I) +(G.5.3), A- 208: (I) + (H.1.1), A-209: (I) + (H.1.2), A-210: (I) +(H.1.3), A-211: (I) + (H.1.4), A-212: (I) + (H.1.5), A- 213: (I) +(H.1.6), A-214: (I) + (H.2.1), A-215: (I) + (H.2.2), A-216: (I) +(H.2.3), A-217: (I) + (H.2.4), A- 218: (I) + (H.2.5), A-219: (I) +(H.2.6), A-220: (I) + (H.2.7), A-221: (I) + (H.2.8), A-222: (I) +(H.2.9), A- 223: (I) + (H.3.1), A-224: (I) + (H.3.2), A-225: (I) +(H.3.3), A-226: (I) + (H.3.4), A-227: (I) + (H.3.5), A- 228: (I) +(H.3.6), A-229: (I) + (H.3.7), A-230: (I) + (H.3.8), A-231: (I) +(H.3.9), A-232: (I) + (H.3.10), A- 233: (I) + (H.3.11), A-234: (I) +(H.4.1), A-235: (I) + (H.4.2), A-236: (I) + (H.4.3), A-237: (I) +(H.4.4), A- 238: (I) + (H.4.5), A-239: (I) + (H.4.6), A-240: (I) +(H.4.7), A-241: (I) + (H.4.8), A-242: (I) + (H.4.9), A- 243: (I) +(H.4.10), A-244: (I) + (I.1.1), A-245: (I) + (I.1.2), A-246: (I) +(I.2.1), A-247: (I) + (I.2.2), A- 248: (I) + (I.2.3), A-249: (I) +(I.2.4), A-250: (I) + (I.2.5), A-251: (I) + (J.1.1), A-252: (I) +(J.1.2), A-253: (I) + (J.1.3), A-254: (I) + (J.1.4), A-255: (I) +(J.1.5), A-256: (I) + (J.1.6), A-257: (I) + (J.1.7), A-258: (I) +(J.1.8), A-259: (I) + (J.1.9), A-260: (I) + (J.1.10), A-261: (I) +(J.1.11), A-262: (I) + (J.1.12), A-263: (I) + (K.1.1), A-264: (I) +(K.1.2), A-265: (I) + (K.1.3), A-266: (I) + (K.1.4), A-267: (I) + (K.1.5), A-268: (I) + (K.1.6), A-269: (I) + (K.1.7), A-270: (I) + (K.1.8),A-271: (I) + (K.1.9), A-272: (I) + (K. 1.10), A-273: (I) + (K.1.11),A-274: (I) + (K.1.12), A-275: (I) + (K.1.13), 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+(O.27.2), A-632: (I) + (O.27.3), A-633: (I) + (O.27.4), A-634: (I) +(O.27.5), A-635: (I) + (O.27.6), A-636: (I) + (O.27.7), A-637: (I) +(O.27.8), A-638: (I) + (O.27.9), A-639: (I) + (O.27.10), A-640: (I) +(O.27.11), A-641: (I) + (O.27.12), A-642: (I) + (O.27.13), A-643: (I) +(O.27.14), A-644: (I) + (O.27.15), A-645: (I) + (O.27.16), A-646: (I) +(O.27.17), A-647: (I) + (O.27.18), A-648: (I) + (O.27.19), A-649: (I) +(O.27.20), A-650: (I) + (O.27.21), A-651: (I) + (O.27.22), A-652: (I) +(O.27.23), A-653: (I) + (O.27.24), A-654: (I) + (O.27.25), A-655: (I) +(O.27.26), A-656: (I) + (O.27.27), A-657: (I) + (O.27.28), A-658: (I) +(O.27.29), A-659: (I) + (O.27.30), A-660: (I) + (O.27.31), A-661: (I) +(O.27.32), A-662: (I) + (O.27.33), A-663: (I) + (O.27.34), A-664: (I) +(O.27.35), A-665: (I) + (O.27.36), A-666: (I) + (O.27.37), A-667: (I) +(O.27.38), A-668: (I) + (O.27.39), A-669: (I) + (O.27.40), A-670: (I) +(O.27.41), A-671: (I) + (O.27.42), A-672: (I) + (O.27.43), A-673: (I) +(O.27.44), A-674: (I) + (O.27.45), A-675: (I) + (O.27.46), A-676: (I) +(O.27.47), A-677: (I) + (O.27.48), A-678: (I) + (O.27.49), A-679: (I) +(O.27.50), A-680: (I) + (O.27.51), A-681: (I) + (O.27.52), A-682: (I) +(O.27.53), A-683: (I) + (O.27.54), A-684: (I) + (O.27.55), A-685: (I) +(O.27.56), A-686: (I) + (O.27.57), A-687: (I) + (O.27.58), A-688: (I) +(O.27.59), A-689: (I) + (O.27.60), A-690: (I) + (O.27.61), A-691: (I) +(O.27.62), A-692: (I) + (O.27.63), A-693: (I) + (O.27.64), A-694: (I) +(O.27.65), A-695: (I) + (O.27.66), A-696: (I) + (O.27.67), A-697: (I) +(O.27.68), A-698: (I) + (O.27.69), A-699: (I) + (O.27.70), A-700: (I) +(O.27.71), A-701: (I) + (O.27.72), A-702: (I) + (O.27.73), A-703: (I) +(O.27.74), A-704: (I) + (O.27.75), A-705: (I) + (O.27.76), A-706: (I) +(O.27.77), A-707: (I) + (O.27.78), A-708: (I) + (O.27.79), A-709: (I) +(O.27.80), A-710: (I) + (O.27.81), A-711: (I) + (O.27.82), A-712: (I) +(O.27.83), A-713: (I) + (O.27.84), A-714: (I) + (O.27.85), A-715: (I) +(O.27.86), A-716: (I) + (O.27.87), A-717: (I) + (O.27.88), A-718: (I) +(O.27.89), A-719: (I) + (O.27.90), A-720: (I) + (O.27.91), A-721: (I) +(O.27.92), A-722: (I) + (O.27.93), A-723: (I) + (O.27.94), A-724: (I) +(O.27.95), A-725: (I) + (O.27.96), A-726: (I) + (O.27.97), A-727: (I) +(O.27.98), A-728: (I) + (O.27.99), A-729: (I) + (O.27.100), A-730: (I) +(A.1.21a), A-731: (I) + (K.1.46), A-732: (I) + (K.1.48), A-733: (I) +(K.1.49), A-734: (I) + (K.1.50), A-735: (I) + (K.1.51), A-736: (I) +(K.1.52), A-737: (I) + (K.1.53), A- 738: (I) + (K.1.54), A-739: (I) +(A.2.6).

In one embodiment the weight ratio of a component 1) to component 2) inmixtures A-1 to A-739 of Table B is between 100:1 and 1:100, preferablybetween 50:1 and 1:50, more preferably between 20:1 and 1:20,particularly between 5:1 and 1:5; for example 3:1, 1:1 or 1:3.

In one embodiment the weight ratio of component 1) to component 2) isbetween 100:1 and 1:100 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) isbetween 50:1 and 1:50 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) isbetween 20:1 and 1:20 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) isbetween 5:1 and 1:5 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) is3:1 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) is1:1 in mixtures A-1 to A-739 of Table A.

In one embodiment the weight ratio of component 1) to component 2) is1:3 in mixtures A-1 to A-739 of Table A.

In a preferred embodiment the mixtures A-1 to A-739 of Table A and inparticular when the weight ratios of component 1) to component 2) are asdisclosed for these mixtures as herein before mentioned, are usedagainst Phakopsora pachyrhizi and P. meibomiae on soybeans and/oragainst Puccinia triticina, P. striiformis, P. hordei, P. graminis or P.recondita on wheat, barley or rye.

Particularly preferred are the binary mixtures listed in Table B1 toTable B13, for example mixtures B1-1 to B1-161 in table B1, whereincomponent 1) is compound I.A, and wherein component 2) is selected fromcompounds II of groups A) to K), as defined herein.

TABLE B1 B1-1: I.A + (A.1.1), B1-2: I.A + (A.1.4), B1-3: I.A + (A.1.8),B1-4: I.A + (A.1.9), B1-5: I.A + (A.1.10), B1-6: I.A + (A.1.11), B1-7:I.A + (A.1.12), B1-8: I.A + (A.1.13), B1-9: I.A + (A.1.14), B1- 10:I.A + (A.1.17), B1-11: I.A + (A.1.21), B1-12: I.A + (A.1.21a), B1-13:I.A + (A.1.24), B1-14: I.A + (A.1.25), B1-15: I.A + (A.1.26), B1-16:I.A + (A.1.27), B1-17: I.A + (A.1.30), B1-18: I.A + (A.1.31), B1-19:I.A + (A.1.32), B1-20: I.A + (A.1.34), B1-21: I.A + (A.1.35), B1-22:I.A + (A.2.1), B1-23: I.A + (A.2.3), B1-24: I.A + (A.2.4), B1-25: I.A +(A.2.5), B1-26: I.A + (A.2.6), B1-27: I.A + (A.3.2), B1-28: I.A +(A.3.3), B1-29: I.A + (A.3.4), B1-30: I.A + (A.3.7), B1-31: I.A +(A.3.9), B1- 32: I.A + (A.3.11), B1-33: I.A + (A.3.12), B1-34: I.A +(A.3.15), B1-35: I.A + (A.3.16), B1-36: I.A + (A.3.17), B1-37: I.A +(A.3.18), B1-38: I.A + (A.3.19), B1-39: I.A + (A.3.20), B1-40: I.A +(A.3.21), B1-41: I.A + (A.3.22), B1-42: I.A + (A.3.23), B1-43: I.A +(A.3.24), B1-44: I.A + (A.3.25), B1-45: I.A + (A.3.26), B1-46: I.A +(A.3.27), B1-47: I.A + (A.3.28), B1-48: I.A + (A.3.29), B1-49: I.A +(A.3.31), B1-50: I.A + (A.3.32), B1-51: I.A + (A.3.33), B1-52: I.A +(A.3.34), B1-53: I.A + (A.3.35), B1-54: I.A + (A.3.36), B1-55: I.A +(A.3.37), B1-56: I.A + (A.3.38), B1-57: I.A + (A.3.39), B1-58: I.A +(A.4.5), B1-59: I.A + (A.4.11), B1-60: I.A + (B.1.4), B1-61: I.A +(B.1.5), B1-62: I.A + (B.1.8.), B1-63: I.A + (B.1.10), B1-64: I.A +(B.1.11), B1-65: I.A + (B.1.12), B1-66: I.A + (B.1.13), B1-67: I.A +(B.1.17), B1-68: I.A + (B.1.18), B1-69: I.A + (B.1.21), B1-70: I.A +(B.1.22), B1-71: I.A + (B.1.23), B1-72: I.A + (B.1.25), B1-73: I.A +(B.1.26), B1-74: I.A + (B.1.29), B1-75: I.A + (B.1.33), B1-76: I.A +(B.1.34), B1-77: I.A + (B.1.37), B1-78: I.A + (B.1.38), B1-79: I.A +(B.1.43), B1-80: I.A + (B.1.46), B1-81: I.A + (B.2.4), B1-82: I.A +(B.2.5), B1-83: I.A + (B.2.6), B1-84: I.A + (B.2.8), B1-85: I.A +(C.1.1), B1-86: I.A + (C.1.2), B1-87: I.A + (C.1.4), B1-88: I.A +(C.1.5), B1-89: I.A + (C.2.6), B1-90: I.A + (C.2.7), B1- 91: I.A +(C.2.8), B1-92: I.A + (D.1.1), B1-93: I.A + (D.1.2), B1-94: I.A +(D.1.5), B1-95: I.A + (D.2.4), B1-96: I.A + (D.2.6), B1-97: I.A +(D.2.7), B1-98: I.A + (E.1.1), B1-99: I.A + (E.1.3), B1- 100: I.A +(E.2.2), B1-101: I.A + (E.2.3), B1-102: I.A + (F.1.2), B1-103: I.A +(F.1.4), B1-104: I.A + (F.1.5), B1-105: I.A + (G.3.1), B1-106: I.A +(G.3.3), B1-107: I.A + (G.3.6), B1-108: I.A + (G.5.1), B1-109: I.A +(G.5.2), B1-110: I.A + (G.5.3), B1-111: I.A + (G.5.4), B1-112: I.A +(G.5.5), B1-113: I.A + (G.5.6), B1-114: I.A + (G.5.7), B1-115: I.A +(G.5.8), B1-116: I.A + (G.5.9), B1-117: I.A + (G.5.10), B1-118: I.A +(G.5.11), B1-119: I.A + (H.1.5), B1-120: I.A + (H.1.7), B1-121: I.A +(H.2.2), B1-122: I.A + (H.2.3), B1-123: I.A + (H.2.5), B1-124: I.A +(H.2.7), B1-125: I.A + (H.2.8), B1-126: I.A + (H.3.2), B1-127: I.A +(H.3.4), B1-128: I.A + (H.3.5), B1- 129: I.A + (H.4.9), B1-130: I.A +(H.4.10), B1-131: I.A + (I.2.2), B1-132: I.A + (I.2.5), B1-133: I.A +(J.1.2), B1-134: I.A + (J.1.5), B1-135: I.A + (J.1.8), B1-136: I.A +(J.1.11), B1-137: I.A + (J.1.12), B1-138: I.A + (K.1.3), B1-139: I.A +(K.1.29), B1-140: I.A + (K.1.30), B1-141: I.A + (K.1.31), B1-142: I.A +(K.1.32), B1-143: I.A + (K.1.41), B1-144: I.A + (K.1.42), B1-145: I.A +(K.1.44), B1-146: I.A + (K.1.45), B1-147: I.A + (K.1.47), B1-148: I.A +(K.1.49), B1-149: I.A + (K.1.53), B1-150: I.A + (K.1.54), B1-151: I.A +(O.4.2), B1-152: I.A + (O.4.5), B1-153: I.A + (O.4.8), B1-154: I.A +(O.26.2), B1-155: I.A + (O.26.3), B1-156: I.A + (O.26.4), B1-157: I.A +(O.26.5), B1-158: I.A + (O.27.7), B1-159: I.A + (O.27.76), B1-160: I.A +(O.27.78), B1-161: I.A + (O.27.79).

In one embodiment the weight ratio of compound I.A to component 2) inmixtures B1-1 to B1-161 of Table B1 is between 100:1 and 1:100,preferably between 50:1 and 1:50, more preferably between 20:1 and 1:20,particularly between 5:1 and 1:5; for example 3:1, 1:1 or 1:3.

Table B2: Mixtures B2-1 to B2-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.B.

Table B3: Mixtures B3-1 to B3-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.C.

Table B4: Mixtures B4-1 to B4-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.D.

Table B5: Mixtures B5-1 to B5-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.E.

Table B6: Mixtures B6-1 to B6-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.F.

Table B7: Mixtures B7-1 to B7-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.G.

Table B8: Mixtures B8-1 to B8-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.H.

Table B9: Mixtures B9-1 to B9-161 are defined as mixtures B1-1 to B1-161of Table B1, wherein compound I.A in each mixture is replaced withcompound I.J.

Table B10: Mixtures B10-1 to B10-161 are defined as mixtures B1-1 toB1-161 of Table B1, wherein compound I.A in each mixture is replacedwith compound I.K.

Table B11: Mixtures B11-1 to B11-161 are defined as mixtures B1-1 toB1-161 of Table B1, wherein compound I.A in each mixture is replacedwith compound I.L.

Table B12: Mixtures B12-1 to B12-161 are defined as mixtures B1-1 toB1-161 of Table B1, wherein compound I.A in each mixture is replacedwith compound I.M.

Table B13: Mixtures B13-1 to B13-161 are defined as mixtures B1-1 toB1-161 of Table B1, wherein compound I.A in each mixture is replacedwith compound I.N.

In one embodiment the weight ratio of component 1) to component 2) isbetween 100:1 and 1:100 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) isbetween 50:1 and 1:50 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) isbetween 20:1 and 1:20 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) isbetween 5:1 and 1:5 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) is3:1 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) is1:1 in mixtures as defined in Tables B1 to B13.

In one embodiment the weight ratio of component 1) to component 2) is1:3 in mixtures as defined in Tables B1 to B13.

In a preferred embodiment the mixtures as defined in Tables to B13 andin particular when the weight ratios of compound I to component 2) areas disclosed for these mixtures as herein before mentioned, are usedagainst Phakopsora pachyrhizi and P. meibomiae on soybeans and/oragainst Puccinia triticina, P. striiformis, P. hordei, P. graminis or P.recondita on wheat, barley or rye.

Further preferred embodiments E.1 to E.144 listed in Table B14 relate tobinary mixtures as defined in Tables B1 to B13 in particular weightratios of component 1) to component 2).

TABLE B14 Weight ratio component 1) to Embodiment Mixture component 2)E.1 B1-14 100:1 to 1:100 E.2 B1-31 100:1 to 1:100 E.3 B1-71 100:1 to1:100 E.4 B1-78 100:1 to 1:100 E.5 B2-14 100:1 to 1:100 E.6 B2-31 100:1to 1:100 E.7 B2-71 100:1 to 1:100 E.8 B2-78 100:1 to 1:100 E.9 B3-14100:1 to 1:100 E.10 B3-31 100:1 to 1:100 E.11 B3-71 100:1 to 1:100 E.12B3-78 100:1 to 1:100 E.13 B4-14 100:1 to 1:100 E.14 B4-31 100:1 to 1:100E.15 B4-71 100:1 to 1:100 E.16 B4-78 100:1 to 1:100 E.17 B5-14 100:1 to1:100 E.18 B5-31 100:1 to 1:100 E.19 B5-71 100:1 to 1:100 E.20 B5-78100:1 to 1:100 E.21 B6-14 100:1 to 1:100 E.22 B6-31 100:1 to 1:100 E.23B6-71 100:1 to 1:100 E.24 B6-78 100:1 to 1:100 E.25 B1-14 50:1 to 1:50E.26 B1-31 50:1 to 1:50 E.27 B1-71 50:1 to 1:50 E.28 B1-78 50:1 to 1:50E.29 B2-14 50:1 to 1:50 E.30 B2-31 50:1 to 1:50 E.31 B2-71 50:1 to 1:50E.32 B2-78 50:1 to 1:50 E.33 B3-14 50:1 to 1:50 E.34 B3-31 50:1 to 1:50E.35 B3-71 50:1 to 1:50 E.36 B3-78 50:1 to 1:50 E.37 B4-14 50:1 to 1:50E.38 B4-31 50:1 to 1:50 E.39 B4-71 50:1 to 1:50 E.40 B4-78 50:1 to 1:50E.41 B5-14 50:1 to 1:50 E.42 B5-31 50:1 to 1:50 E.43 B5-71 50:1 to 1:50E.44 B5-78 50:1 to 1:50 E.45 B6-14 50:1 to 1:50 E.46 B6-31 50:1 to 1:50E.47 B6-71 50:1 to 1:50 E.48 B6-78 50:1 to 1:50 E.49 B1-14 20:1 to 1:20E.50 B1-31 20:1 to 1:20 E.51 B1-71 20:1 to 1:20 E.52 B1-78 20:1 to 1:20E.53 B2-14 20:1 to 1:20 E.54 B2-31 20:1 to 1:20 E.55 B2-71 20:1 to 1:20E.56 B2-78 20:1 to 1:20 E.57 B3-14 20:1 to 1:20 E.58 B3-31 20:1 to 1:20E.59 B3-71 20:1 to 1:20 E.60 B3-78 20:1 to 1:20 E.61 B4-14 20:1 to 1:20E.62 B4-31 20:1 to 1:20 E.63 B4-71 20:1 to 1:20 E.64 B4-78 20:1 to 1:20E.65 B5-14 20:1 to 1:20 E.66 B5-31 20:1 to 1:20 E.67 B5-71 20:1 to 1:20E.68 B5-78 20:1 to 1:20 E.69 B6-14 20:1 to 1:20 E.70 B6-31 20:1 to 1:20E.71 B6-71 20:1 to 1:20 E.72 B6-78 20:1 to 1:20 E.73 B1-14 5:1 to 1:5E.74 B1-31 5:1 to 1:5 E.75 B1-71 5:1 to 1:5 E.76 B1-78 5:1 to 1:5 E.77B2-14 5:1 to 1:5 E.78 B2-31 5:1 to 1:5 E.79 B2-71 5:1 to 1:5 E.80 B2-785:1 to 1:5 E.81 B3-14 5:1 to 1:5 E.82 B3-31 5:1 to 1:5 E.83 B3-71 5:1 to1:5 E.84 B3-78 5:1 to 1:5 E.85 B4-14 5:1 to 1:5 E.86 B4-31 5:1 to 1:5E.87 B4-71 5:1 to 1:5 E.88 B4-78 5:1 to 1:5 E.89 B5-14 5:1 to 1:5 E.90B5-31 5:1 to 1:5 E.91 B5-71 5:1 to 1:5 E.92 B5-78 5:1 to 1:5 E.93 B6-145:1 to 1:5 E.94 B6-31 5:1 to 1:5 E.95 B6-71 5:1 to 1:5 E.96 B6-78 5:1 to1:5 E.97 B1-14 3:1 to 1:3 E.98 B1-31 3:1 to 1:3 E.99 B1-71 3:1 to 1:3E.100 B1-78 3:1 to 1:3 E.101 B2-14 3:1 to 1:3 E.102 B2-31 3:1 to 1:3E.103 B2-71 3:1 to 1:3 E.104 B2-78 3:1 to 1:3 E.105 B3-14 3:1 to 1:3E.106 B3-31 3:1 to 1:3 E.107 B3-71 3:1 to 1:3 E.108 B3-78 3:1 to 1:3E.109 B4-14 3:1 to 1:3 E.110 B4-31 3:1 to 1:3 E.111 B4-71 3:1 to 1:3E.112 B4-78 3:1 to 1:3 E.113 B5-14 3:1 to 1:3 E.114 B5-31 3:1 to 1:3E.115 B5-71 3:1 to 1:3 E.116 B5-78 3:1 to 1:3 E.117 B6-14 3:1 to 1:3E.118 B6-31 3:1 to 1:3 E.119 B6-71 3:1 to 1:3 E.120 B6-78 3:1 to 1:3E.121 B1-14 1:1 E.122 B1-31 1:1 E.123 B1-71 1:1 E.124 B1-78 1:1 E.125B2-14 1:1 E.126 B2-31 1:1 E.127 B2-71 1:1 E.128 B2-78 1:1 E.129 B3-141:1 E.130 B3-31 1:1 E.131 B3-71 1:1 E.132 B3-78 1:1 E.133 B4-14 1:1E.134 B4-31 1:1 E.135 B4-71 1:1 E.136 B4-78 1:1 E.137 B5-14 1:1 E.138B5-31 1:1 E.139 B5-71 1:1 E.140 B5-78 1:1 E.141 B6-14 1:1 E.142 B6-311:1 E.143 B6-71 1:1 E.144 B6-78 1:1

A preferred embodiment relates to the use of the mixtures according toembodiments E.1 to E.144 of Table B14 against Phakopsora pachyrhizi andP. meibomiae on soybeans and/or against Puccinia triticina, P.striiformis, P. hordei, P. graminis or P. recondita on wheat, barley orrye.

It may be preferred that the binary mixtures above comprise besides atleast one compound I and at least one compound as component 3) at leastone further active compound III, resulting in a ternary mixture.Preferably, the components 1) and 2), or, all three components 1), 2)and 3), in these mixtures are present in a synergistically effectiveamount.

Accordingly one embodiment relates to ternary mixtures comprising, asactive components

-   1) at least one active compound I as defined or preferably defined    herein, or an N-oxide, or an agriculturally useful salt thereof;    and as component-   2) at least one active compound selected from groups A) to O) as    defined for component 2) in binary mixtures above, or an N-oxide, or    an agriculturally useful salt thereof; and as component-   3) at least one active compound III selected from groups A) to O) as    defined for component 2) in binary mixtures above, or an N-oxide, or    an agriculturally useful salt thereof;    wherein the at least one active compound III of component 3) is not    identical with the at least one active compound II of component 2).

The invention also relates to a method for controlling phytopathogenicharmful fungi using the abovementioned ternary mixtures; to agrochemicalcompositions comprising these ternary mixtures; and to agrochemicalcompositions further comprising seed comprising these mixtures.

It is preferred that the ternary mixtures comprise as compounds IIIfungicidal compounds that are independently of each other selected fromthe groups A), B), C), D), E), F), G), H), I), J), K) and O); andwherein the at least one active compound III of component 3) is notidentical with the at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from inhibitors of complex III at Q_(o) site in groupA), more preferably selected from compounds (A.1.1), (A.1.4), (A.1.8),(A.1.9), (A.1.10), (A.1.11), (A.1.12), (A.1.13), (A.1.14), (A.1.17),(A.1.21), (A.1.21a), (A.1.24), (A.1.25), (A.1.26), (A.1.27), (A.1.30),(A.1.31), (A.1.32), (A.1.34) and (A.1.35); particularly selected from(A.1.1), (A.1.8), (A.1.9), (A.1.10), (A.1.11), (A.1.13), (A.1.14),(A.1.17), (A.1.25), and (A.1.34); and wherein the at least one activecompound III of component 3) is not identical with the at least oneactive compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from inhibitors of complex III at Q_(i) site in groupA), more preferably selected from compounds (A.2.1), (A.2.3), (A.2.4),(A.2.5) and (A.2.6); particularly selected from (A.2.4) and (A.2.6); andwherein the at least one active compound III of component 3) is notidentical with the at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from inhibitors of complex II in group A), morepreferably selected from compounds (A.3.2), (A.3.3), (A.3.4), (A.3.7),(A.3.9), (A.3.11), (A.3.12), (A.3.15), (A.3.16), (A.3.17), (A.3.18),(A.3.19), (A.3.20), (A.3.21), (A.3.22), (A.3.23), (A.3.24), (A.3.25),(A.3.26), (A.3.27), (A.3.28), (A.3.29), (A.3.31), (A.3.32), (A.3.33),(A.3.34), (A.3.35), (A.3.36), (A.3.37), (A.3.38) and (A.3.39);particularly selected from (A.3.2), (A.3.3), (A.3.4), (A.3.7), (A.3.9),(A.3.17), (A.3.24), (A.3.28), (A.3.29), (A.3.31), (A.3.32), (A.3.33),(A.3.34), (A.3.35), (A.3.36), (A.3.37), (A.3.38) and (A.3.39); andwherein the at least one active compound III of component 3) is notidentical with the at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from other respiration inhibitors in group A), morepreferably selected from compounds (A.4.5) and (A.4.11); and wherein theat least one active compound III of component 3) is not identical withthe at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from C14 demethylase inhibitors in group B), morepreferably selected from compounds (B.1.4), (B.1.5), (B.1.8), (B.1.10),(B.1.11), (B.1.12), (B.1.13), (B.1.17), (B.1.18), (B.1.21), (B.1.22),(B.1.23), (B.1.25), (B.1.26), (B.1.29), (B.1.33), (B.1.34), (B.1.37),(B.1.38), (B.1.43) and (B.1.46); particularly selected from (B.1.4),(B.1.5), (B.1.8), (B.1.17), (B.1.22), (B.1.23), (B.1.25), (B.1.29), and(B.1.38); and wherein the at least one active compound III of component3) is not identical with the at least one active compound II ofcomponent 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from Delta14-reductase inhibitors in group B), morepreferably selected from compounds (B.2.4), (B.2.5), (B.2.6) and(B.2.8); in particular (B.2.4) and (B.2.6); and wherein the at least oneactive compound III of component 3) is not identical with the at leastone active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from phenylamides and acyl amino acid fungicides ingroup C), more preferably selected from compounds (C.1.1), (C.1.2),(C.1.4) and (C.1.5); and wherein the at least one active compound III ofcomponent 3) is not identical with the at least one active compound IIof component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from other nucleic acid synthesis inhibitors in groupC), more preferably selected from compounds (C.2.6), (C.2.7) and(C.2.8); and wherein the at least one active compound III of component3) is not identical with the at least one active compound II ofcomponent 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group D), more preferably selected from compounds(D.1.1), (D.1.2), (D.1.5), (D.2.4), (D.2.6) and (D.2.7); particularlyselected from (D.2.6) and (D.2.7); and wherein the at least one activecompound Ill of component 3) is not identical with the at least oneactive compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group E), more preferably selected from compounds(E.1.1), (E.1.3), (E.2.2) and (E.2.3); in particular (E.1.1); andwherein the at least one active compound III of component 3) is notidentical with the at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group F), more preferably selected from compounds(F.1.2), (F.1.4) and (F.1.5); and wherein the at least one activecompound III of component 3) is not identical with the at least oneactive compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group G), more preferably selected from compounds(G.3.1), (G.3.3), (G.3.6), (G.5.1), (G.5.2), (G.5.3), (G.5.4), (G.5.5),(G.5.6), G.5.7), (G.5.8), (G.5.9), (G.5.10) and (G.5.11); and whereinthe at least one active compound III of component 3) is not identicalwith the at least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group H), more preferably selected from compounds(H.1.5), (H.1.7), (H.2.2), (H.2.3), (H.2.5), (H.2.7), (H.2.8), (H.3.2),(H.3.4), (H.3.5), (H.4.9) and (H.4.10); particularly selected from(H.1.5), (H.1.7), (H.2.2), (H.3.2) and (H.3.5); and wherein the at leastone active compound III of component 3) is not identical with the atleast one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group 1), more preferably selected from compounds(I.2.2) and (I.2.5); and wherein the at least one active compound III ofcomponent 3) is not identical with the at least one active compound IIof component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group J), more preferably selected from compounds(J.1.2), (J.1.5), (J.1.8), (J.1.11) and (J.1.12); and wherein the atleast one active compound III of component 3) is not identical with theat least one active compound II of component 2).

Preference is also given to ternary mixtures based on binary mixturesdisclosed herein, comprising as component 3) at least one activecompound selected from group K), more preferably selected from compounds(K.1.3), (K.1.29), (K.1.30), (K.1.31), (K.1.32), (K.1.41), (K.1.42),(K.1.44), (K.1.45), (K.1.47), (K.1.49), (K.1.53) and (K.1.54);particularly selected from (K.1.3), (K.1.29), (K.1.30), (K.1.31),(K.1.32), (K.1.42), (K.1.53) and (K.1.54); and wherein the at least oneactive compound III of component 3) is not identical with the at leastone active compound II of component 2).

The present invention relates furthermore to the mixtures as defined inTables C1 to C6 comprising as component 1) one of the compounds I.A,I.B, I.C, I.D, I.E, I.F, I.G, I.H, I.J, I.K, I.L, I.M or I.N as definedabove, and as component 2) one of the compounds as defined and numberedabove from groups A) to K), and as component 3) a compound III fromgroups A) to K) as defined herein. Preferably, the compositions comprisethe active substances in synergistically effective amounts.

TABLE C1 Ternary mixtures C1-1 to C1-6865 comprising compound I.A asdefined herein as component 1) and one compound II as defined above ascomponent 2) and one compound III as defined above as component 3). Thecomponents 1), 2) and 3) are written down in this order (comp. 1) +comp. 2) + comp. 3)), so that one mixture, for example mixture C1-1,comprises as component 1) compound I.A, as component 2) compound (A.1.4)and as component 3) compound (A.1.1). C1-1: I.A + (A.1.4) + (A.1.1),C1-2: I.A + (A.1.8) + (A.1.1), C1-3: I.A + (A.1.9) + (A.1.1), C1-4:I.A + (A.1.10) + (A.1.1), C1-5: I.A + (A.1.11) + (A.1.1), C1-6: I.A +(A.1.12) + (A.1.1), C1-7: I.A + (A.1.13) + (A.1.1), C1-8: I.A +(A.1.14) + (A.1.1), C1-9: I.A + (A.1.17) + (A.1.1), C1-10: I.A +(A.1.21) + (A.1.1), C1-11: I.A + (A.1.21a) + (A.1.1), C1-12: I.A +(A.1.24) + (A.1.1), C1-13: I.A + (A.1.25) + (A.1.1), C1-14: I.A +(A.1.26) + (A.1.1), C1-15: I.A + (A.1.27) + (A.1.1), C1-16: I.A +(A.1.30) + (A.1.1), C1-17: I.A + (A.1.31) + (A.1.1), C1-18: I.A +(A.1.32) + (A.1.1), C1-19: I.A + (A.1.34) + (A.1.1), C1-20: I.A +(A.1.35) + (A.1.1), C1-21: I.A + (A.2.1) + (A.1.1), C1-22: I.A +(A.2.3) + (A.1.1), C1-23: I.A + (A.2.4) + (A.1.1), C1-24: I.A +(A.2.5) + (A.1.1), C1-25: I.A + (A.2.6) + (A.1.1), C1-26: I.A +(A.3.2) + (A.1.1), C1-27: I.A + (A.3.3) + (A.1.1), C1-28: I.A +(A.3.4) + (A.1.1), C1-29: I.A + (A.3.7) + (A.1.1), C1-30: I.A +(A.3.9) + (A.1.1), C1-31: I.A + (A.3.11) + (A.1.1), C1-32: I.A +(A.3.12) + (A.1.1), C1-33: I.A + (A.3.15) + (A.1.1), C1-34: I.A +(A.3.16) + (A.1.1), C1-35: I.A + (A.3.17) + (A.1.1), C1-36: I.A +(A.3.18) + (A.1.1), C1-37: I.A + (A.3.19) + (A.1.1), C1-38: I.A +(A.3.20) + (A.1.1), C1-39: I.A + (A.3.21) + (A.1.1), C1-40: I.A +(A.3.22) + (A.1.1), C1-41: I.A + (A.3.23) + (A.1.1), C1-42: I.A +(A.3.24) + (A.1.1), C1-43: I.A + (A.3.25) + (A.1.1), C1-44: I.A +(A.3.26) + (A.1.1), C1-45: I.A + (A.3.27) + (A.1.1), C1-46: I.A +(A.3.28) + (A.1.1), C1-47: I.A + (A.3.29) + (A.1.1), C1-48: I.A +(A.3.31) + (A.1.1), C1-49: I.A + (A.3.32) + (A.1.1), C1-50: I.A +(A.3.33) + (A.1.1), C1-51: I.A + (A.3.34) + (A.1.1), C1-52: I.A +(A.3.35) + (A.1.1), C1-53: I.A + (A.3.36) + (A.1.1), C1-54: I.A +(A.3.37) + (A.1.1), C1-55: I.A + (A.3.38) + (A.1.1), C1-56: I.A +(A.3.39) + (A.1.1), C1-57: I.A + (A.4.5) + (A.1.1), C1-58: I.A +(A.4.11) + (A.1.1), C1-59: I.A + (B.1.4) + (A.1.1), C1-60: I.A +(B.1.5) + (A.1.1), C1-61: I.A + (B.1.8.) + (A.1.1), C1-62: I.A +(B.1.10) + (A.1.1), C1-63: I.A + (B.1.11) + (A.1.1), C1-64: I.A +(B.1.12) + (A.1.1), C1-65: I.A + (B.1.13) + (A.1.1), C1-66: I.A +(B.1.17) + (A.1.1), C1-67: I.A + (B.1.18) + (A.1.1), C1-68: I.A +(B.1.21) + (A.1.1), C1-69: I.A + (B.1.22) + (A.1.1), C1-70: I.A +(B.1.23) + (A.1.1), C1-71: I.A + (B.1.25) + (A.1.1), C1-72: I.A +(B.1.26) + (A.1.1), C1-73: I.A + (B.1.29) + (A.1.1), C1-74: I.A +(B.1.33) + (A.1.1), C1-75: I.A + (B.1.34) + (A.1.1), C1-76: I.A +(B.1.37) + (A.1.1), C1-77: I.A + (B.1.38) + (A.1.1), C1-78: I.A +(B.1.43) + (A.1.1), C1-79: I.A + (B.1.46) + (A.1.1), C1-80: I.A +(B.2.4) + (A.1.1), C1-81: I.A + (B.2.5) + (A.1.1), C1-82: I.A +(B.2.6) + (A.1.1), C1-83: I.A + (B.2.8) + (A.1.1), C1-84: I.A +(C.1.1) + (A.1.1), C1-85: I.A + (C.1.2) + (A.1.1), C1-86: I.A +(C.1.4) + (A.1.1), C1-87: I.A + (C.1.5) + (A.1.1), C1-88: I.A +(C.2.6) + (A.1.1), C1-89: I.A + (C.2.7) + (A.1.1), C1-90: I.A +(C.2.8) + (A.1.1), C1-91: I.A + (D.1.1) + (A.1.1), C1-92: I.A +(D.1.2) + (A.1.1), C1-93: I.A + (D.1.5) + (A.1.1), C1-94: I.A +(D.2.4) + (A.1.1), C1-95: I.A + (D.2.6) + (A.1.1), C1-96: I.A +(D.2.7) + (A.1.1), C1-97: I.A + (E.1.1) + (A.1.1), C1-98: I.A +(E.1.3) + (A.1.1), C1-99: I.A + (E.2.2) + (A.1.1), C1-100: I.A +(E.2.3) + (A.1.1), C1-101: I.A + (F.1.2) + (A.1.1), C1-102: I.A +(F.1.4) + (A.1.1), C1-103: I.A + (F.1.5) + (A.1.1), C1-104: I.A +(G.3.1) + (A.1.1), C1-105: I.A + (G.3.3) + (A.1.1), C1-106: I.A +(G.3.6) + (A.1.1), C1-107: I.A + (G.5.1) + (A.1.1), C1-108: I.A +(G.5.2) + (A.1.1), C1-109: I.A + (G.5.3) + (A.1.1), C1-110: I.A +(G.5.4) + (A.1.1), C1-111: I.A + (G.5.5) + (A.1.1), C1-112: I.A +(G.5.6) + (A.1.1), C1-113: I.A + (G.5.7) + (A.1.1), C1-114: I.A +(G.5.8) + (A.1.1), C1-115: I.A + (G.5.9) + (A.1.1), C1-116: I.A +(G.5.10) + (A.1.1), C1-117: I.A + (G.5.11) + (A.1.1), C1-118: I.A +(H.1.5) + (A.1.1), C1-119: I.A + (H.1.7) + (A.1.1), C1-120: I.A +(H.2.2) + (A.1.1), C1-121: I.A + (H.2.3) + (A.1.1), C1-122: I.A +(H.2.5) + (A.1.1), C1-123: I.A + (H.2.7) + (A.1.1), C1-124: I.A +(H.2.8) + (A.1.1), C1-125: I.A + (H.3.2) + (A.1.1), C1-126: I.A +(H.3.4) + (A.1.1), C1-127: I.A + (H.3.5) + (A.1.1), C1-128: I.A +(H.4.9) + (A.1.1), C1-129: I.A + (H.4.10) + (A.1.1), C1-130: I.A +(I.2.2) + (A.1.1), C1-131: I.A + (I.2.5) + (A.1.1), C1-132: I.A +(J.1.2) + (A.1.1), C1-133: I.A + (J.1.5) + (A.1.1), C1-134: I.A +(J.1.8) + (A.1.1), C1-135: I.A + (J.1.11) + (A.1.1), C1-136: I.A +(J.1.12) + (A.1.1), C1-137: I.A + (K.1.3) + (A.1.1), C1-138: I.A +(K.1.29) + (A.1.1), C1-139: I.A + (K.1.30) + (A.1.1), C1-140: I.A +(K.1.31) + (A.1.1), C1-141: I.A + (K.1.32) + (A.1.1), C1-142: I.A +(K.1.41) + (A.1.1), C1-143: I.A + (K.1.42) + (A.1.1), C1-144: I.A +(K.1.44) + (A.1.1), C1-145: I.A + (K.1.45) + (A.1.1), C1-146: I.A +(K.1.47) + (A.1.1), C1-147: I.A + (K.1.49) + (A.1.1), C1- 148: I.A +(K.1.53) + (A.1.1), C1-149: I.A + (K.1.54) + (A.1.1), C1-150: I.A +(A.1.4) + (A.1.8), C1-151: I.A + (A.1.9) + (A.1.8), C1-152: I.A +(A.1.10) + (A.1.8), C1-153: I.A + (A.1.11) + (A.1.8), C1-154: I.A +(A.1.12) + (A.1.8), C1-155: I.A + (A.1.13) + (A.1.8), C1-156: I.A +(A.1.14) + (A.1.8), C1-157: I.A + (A.1.17) + (A.1.8), C1-158: I.A +(A.1.21) + (A.1.8), C1-159: I.A + (A.1.21a) + (A.1.8), C1-160: I.A +(A.1.24) + (A.1.8), C1-161: I.A + (A.1.25) + (A.1.8), C1-162: I.A +(A.1.26) + (A.1.8), C1-163: I.A + (A.1.27) + (A.1.8), C1-164: I.A +(A.1.30) + (A.1.8), C1- 165: I.A + (A.1.31) + (A.1.8), C1-166: I.A +(A.1.32) + (A.1.8), C1-167: I.A + (A.1.34) + (A.1.8), C1-168: I.A +(A.1.35) + (A.1.8), C1-169: I.A + (A.2.1) + (A.1.8), C1-170: I.A +(A.2.3) + (A.1.8), C1-171: I.A + (A.2.4) + (A.1.8), C1-172: I.A +(A.2.5) + (A.1.8), C1-173: I.A + (A.2.6) + (A.1.8), C1-174: I.A +(A.3.2) + (A.1.8), C1-175: I.A + (A.3.3) + (A.1.8), C1-176: I.A +(A.3.4) + (A.1.8), C1-177: I.A + (A.3.7) + (A.1.8), C1-178: I.A +(A.3.9) + (A.1.8), C1-179: I.A + (A.3.11) + (A.1.8), C1-180: I.A +(A.3.12) + (A.1.8), C1-181: I.A + (A.3.15) + (A.1.8), C1-182: I.A +(A.3.16) + (A.1.8), C1-183: I.A + (A.3.17) + (A.1.8), C1-184: I.A +(A.3.18) + (A.1.8), C1-185: I.A + 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C1-1760:I.A + (B.1.10) + (A.3.2), C1-1761: I.A + (B.1.11) + (A.3.2), C1-1762:I.A + (B.1.12) + (A.3.2), C1-1763: I.A + (B.1.13) + (A.3.2), C1-1764:I.A + (B.1.17) + (A.3.2), C1-1765: I.A + (B.1.18) + (A.3.2), C1-1766:I.A + (B.1.21) + (A.3.2), C1-1767: I.A + (B.1.22) + (A.3.2), C1-1768:I.A + (B.1.23) + (A.3.2), C1-1769: I.A + (B.1.25) + (A.3.2), C1-1770:I.A + (B.1.26) + (A.3.2), C1-1771: I.A + (B.1.29) + (A.3.2), C1- 1772:I.A + (B.1.33) + (A.3.2), C1-1773: I.A + (B.1.34) + (A.3.2), C1-1774:I.A + (B.1.37) + (A.3.2), C1-1775: I.A + (B.1.38) + (A.3.2), C1-1776:I.A + (B.1.43) + (A.3.2), C1-1777: I.A + (B.1.46) + (A.3.2), C1-1778:I.A + (B.2.4) + (A.3.2), C1-1779: I.A + (B.2.5) + (A.3.2), C1-1780:I.A + (B.2.6) + (A.3.2), C1-1781: I.A + (B.2.8) + (A.3.2), C1-1782:I.A + (C.1.1) + (A.3.2), C1- 1783: I.A + (C.1.2) + (A.3.2), C1-1784:I.A + (C.1.4) + (A.3.2), C1-1785: I.A + (C.1.5) + (A.3.2), C1-1786:I.A + (C.2.6) + (A.3.2), C1-1787: I.A + (C.2.7) + (A.3.2), C1-1788:I.A + (C.2.8) + (A.3.2), C1-1789: I.A + (D.1.1) + (A.3.2), C1-1790:I.A + (D.1.2) + (A.3.2), C1-1791: I.A + (D.1.5) + (A.3.2), C1-1792:I.A + (D.2.4) + (A.3.2), C1-1793: I.A + (D.2.6) + (A.3.2), C1-1794:I.A + (D.2.7) + (A.3.2), C1-1795: I.A + (E.1.1) + (A.3.2), C1-1796:I.A + (E.1.3) + (A.3.2), C1-1797: I.A + (E.2.2) + (A.3.2), C1-1798:I.A + (E.2.3) + (A.3.2), C1-1799: I.A + (F.1.2) + (A.3.2), C1-1800:I.A + (F.1.4) + (A.3.2), C1-1801: I.A + (F.1.5) + (A.3.2), C1-1802:I.A + (G.3.1) + (A.3.2), C1- 1803: I.A + (G.3.3) + (A.3.2), C1-1804:I.A + (G.3.6) + (A.3.2), C1-1805: I.A + (G.5.1) + (A.3.2), C1-1806:I.A + (G.5.2) + (A.3.2), C1-1807: I.A + (G.5.3) + (A.3.2), C1-1808:I.A + (G.5.4) + (A.3.2), C1-1809: I.A + (G.5.5) + (A.3.2), C1-1810:I.A + (G.5.6) + (A.3.2), C1-1811: I.A + (G.5.7) + (A.3.2), C1-1812:I.A + (G.5.8) + (A.3.2), C1-1813: I.A + (G.5.9) + (A.3.2), C1-1814:I.A + (G.5.10) + (A.3.2), C1-1815: I.A + (G.5.11) + (A.3.2), C1-1816:I.A + (H.1.5) + (A.3.2), C1- 1817: I.A + (H.1.7) + (A.3.2), C1-1818:I.A + (H.2.2) + (A.3.2), C1-1819: I.A + (H.2.3) + (A.3.2), C1-1820:I.A + (H.2.5) + (A.3.2), C1-1821: I.A + (H.2.7) + (A.3.2), C1-1822:I.A + (H.2.8) + (A.3.2), C1-1823: I.A + (H.3.2) + (A.3.2), C1-1824:I.A + (H.3.4) + (A.3.2), C1-1825: I.A + (H.3.5) + (A.3.2), C1-1826:I.A + (H.4.9) + (A.3.2), C1-1827: I.A + (H.4.10) + (A.3.2), C1-1828:I.A + (I.2.2) + (A.3.2), C1-1829: I.A + (I.2.5) + (A.3.2), C1-1830:I.A + (J.1.2) + (A.3.2), C1-1831: I.A + (J.1.5) + (A.3.2), C1-1832:I.A + (J.1.8) + (A.3.2), C1-1833: I.A + (J.1.11) + (A.3.2), C1-1834:I.A + (J.1.12) + (A.3.2), C1-1835: I.A + (K.1.3) + (A.3.2), C1-1836:I.A + (K.1.29) + (A.3.2), C1- 1837: I.A + (K.1.30) + (A.3.2), C1-1838:I.A + (K.1.31) + (A.3.2), C1-1839: I.A + (K.1.32) + (A.3.2), C1-1840:I.A + (K.1.41) + (A.3.2), C1-1841: I.A + (K.1.42) + (A.3.2), C1-1842:I.A + (K.1.44) + (A.3.2), C1-1843: I.A + (K.1.45) + (A.3.2), C1-1844:I.A + (K.1.47) + (A.3.2), C1-1845: I.A + (K.1.49) + (A.3.2), C1-1846:I.A + (K.1.53) + (A.3.2), C1-1847: I.A + (K.1.54) + (A.3.2), C1- 1848:I.A + (A.1.4) + (A.3.3), C1-1849: I.A + (A.1.12) + (A.3.3), C1-1850:I.A + (A.1.21) + (A.3.3), C1-1851: I.A + (A.1,21a) + (A.3.3), C1-1852:I.A + (A.1.24) + (A.3.3), C1-1853: I.A + (A.1.26) + (A.3.3), C1-1854:I.A + (A.1.27) + (A.3.3), C1-1855: I.A + (A.1.30) + (A.3.3), C1-1856:I.A + (A.1.31) + (A.3.3), C1-1857: I.A + (A.1.32) + (A.3.3), C1-1858:I.A + (A.1.35) + (A.3.3), C1- 1859: I.A + (A.2.1) + (A.3.3), C1-1860:I.A + (A.2.3) + (A.3.3), C1-1861: I.A + (A.2.5) + (A.3.3), C1-1862:I.A + (A.3.4) + (A.3.3), C1-1863: I.A + (A.3.7) + (A.3.3), C1-1864:I.A + (A.3.9) + (A.3.3), C1-1865: I.A + (A.3.11) + (A.3.3), C1-1866:I.A + (A.3.12) + (A.3.3), C1-1867: I.A + (A.3.15) + (A.3.3), C1-1868:I.A + (A.3.16) + (A.3.3), C1-1869: I.A + (A.3.17) + (A.3.3), C1-1870:I.A + (A.3.18) + (A.3.3), C1-1871: I.A + (A.3.19) + (A.3.3), C1-1872:I.A + (A.3.20) + (A.3.3), C1- 1873: I.A + (A.3.21) + (A.3.3), C1-1874:I.A + (A.3.22) + (A.3.3), C1-1875: I.A + (A.3.23) + (A.3.3), C1-1876:I.A + (A.3.24) + (A.3.3), C1-1877: I.A + (A.3.25) + (A.3.3), C1-1878:I.A + (A.3.26) + (A.3.3), C1-1879: I.A + (A.3.27) + (A.3.3), C1-1880:I.A + (A.3.28) + (A.3.3), C1-1881: I.A + (A.3.29) + (A.3.3), C1-1882:I.A + (A.3.31) + (A.3.3), C1-1883: I.A + (A.3.32) + (A.3.3), C1- 1884:I.A + (A.3.33) + (A.3.3), C1-1885: I.A + (A.3.34) + (A.3.3), C1-1886:I.A + (A.3.35) + (A.3.3), C1-1887: I.A + (A.3.36) + (A.3.3), C1-1888:I.A + (A.3.37) + (A.3.3), C1-1889: I.A + (A.3.38) + (A.3.3), C1-1890:I.A + (A.3.39) + (A.3.3), C1-1891: I.A + (A.4.5) + (A.3.3), C1-1892:I.A + (A.4.11) + (A.3.3), C1-1893: I.A + (B.1.4) + (A.3.3), C1-1894:I.A + (B.1.5) + (A.3.3), C1- 1895: I.A + (B.1.8.) + (A.3.3), C1-1896:I.A + (B.1.10) + (A.3.3), C1-1897: I.A + (B.1.11) + (A.3.3), C1-1898:I.A + (B.1.12) + (A.3.3), C1-1899: I.A + (B.1.13) + (A.3.3), C1-1900:I.A + (B.1.17) + (A.3.3), C1-1901: I.A + (B.1.18) + (A.3.3), C1-1902:I.A + (B.1.21) + (A.3.3), C1-1903: I.A + (B.1.22) + (A.3.3), C1-1904:I.A + (B.1.23) + (A.3.3), C1-1905: I.A + (B.1.25) + (A.3.3), C1- 1906:I.A + (B.1.26) + (A.3.3), C1-1907: I.A + (B.1.29) + (A.3.3), C1-1908:I.A + (B.1.33) + (A.3.3), C1-1909: I.A + (B.1.34) + (A.3.3), C1-1910:I.A + (B.1.37) + (A.3.3), C1-1911: I.A + (B.1.38) + (A.3.3), C1-1912:I.A + (B.1.43) + (A.3.3), C1-1913: I.A + (B.1.46) + (A.3.3), C1-1914:I.A + (B.2.4) + (A.3.3), C1-1915: I.A + (B.2.5) + (A.3.3), C1-1916:I.A + (B.2.6) + (A.3.3), C1- 1917: I.A + (B.2.8) + (A.3.3), C1-1918:I.A + (C.1.1) + (A.3.3), C1-1919: I.A + (C.1.2) + (A.3.3), C1-1920:I.A + (C.1.4) + (A.3.3), C1-1921: I.A + (C.1.5) + (A.3.3), C1-1922:I.A + (C.2.6) + (A.3.3), C1-1923: I.A + (C.2.7) + (A.3.3), C1-1924:I.A + (C.2.8) + (A.3.3), C1-1925: I.A + (D.1.1) + (A.3.3), C1-1926:I.A + (D.1.2) + (A.3.3), C1-1927: I.A + (D.1.5) + (A.3.3), C1-1928:I.A + (D.2.4) + (A.3.3), C1-1929: I.A + (D.2.6) + (A.3.3), C1-1930:I.A + (D.2.7) + (A.3.3), C1-1931: I.A + (E.1.1) + (A.3.3), C1-1932:I.A + (E.1.3) + (A.3.3), C1-1933: I.A + (E.2.2) + (A.3.3), C1-1934:I.A + (E.2.3) + (A.3.3), C1-1935: I.A + (F.1.2) + (A.3.3), C1-1936:I.A + (F.1.4) + (A.3.3), C1- 1937: I.A + (F.1.5) + (A.3.3), C1-1938:I.A + (G.3.1) + (A.3.3), C1-1939: I.A + (G.3.3) + (A.3.3), C1-1940:I.A + (G.3.6) + (A.3.3), C1-1941: I.A + (G.5.1) + (A.3.3), C1-1942:I.A + (G.5.2) + (A.3.3), C1-1943: I.A + (G.5.3) + (A.3.3), C1-1944:I.A + (G.5.4) + (A.3.3), C1-1945: I.A + (G.5.5) + (A.3.3), C1-1946:I.A + (G.5.6) + (A.3.3), C1-1947: I.A + (G.5.7) + (A.3.3), C1-1948:I.A + (G.5.8) + (A.3.3), C1-1949: I.A + (G.5.9) + (A.3.3), C1-1950:I.A + (G.5.10) + (A.3.3), C1- 1951: I.A + (G.5.11) + (A.3.3), C1-1952:I.A + (H.1.5) + (A.3.3), C1-1953: I.A + (H.1.7) + (A.3.3), C1-1954:I.A + (H.2.2) + (A.3.3), C1-1955: I.A + (H.2.3) + (A.3.3), C1-1956:I.A + (H.2.5) + (A.3.3), C1-1957: I.A + (H.2.7) + (A.3.3), C1-1958:I.A + (H.2.8) + (A.3.3), C1-1959: I.A + (H.3.2) + (A.3.3), C1-1960:I.A + (H.3.4) + (A.3.3), C1-1961: I.A + (H.3.5) + (A.3.3), C1-1962:I.A + (H.4.9) + (A.3.3), C1-1963: I.A + (H.4.10) + (A.3.3), C1-1964:I.A + (I.2.2) + (A.3.3), C1-1965: I.A + (I.2.5) + (A.3.3), C1-1966:I.A + (J.1.2) + (A.3.3), C1-1967: I.A + (J.1.5) + (A.3.3), C1-1968:I.A + (J.1.8) + (A.3.3), C1-1969: I.A + (J.1.11) + (A.3.3), C1-1970:I.A + (J.1.12) + (A.3.3), C1-1971: I.A + (K.1.3) + (A.3.3), C1-1972:I.A + (K.1.29) + (A.3.3), C1-1973: I.A + (K.1.30) + (A.3.3), C1- 1974:I.A + (K.1.31) + (A.3.3), C1-1975: I.A + (K.1.32) + (A.3.3), C1-1976:I.A + (K.1.41) + (A.3.3), C1-1977: I.A + (K.1.42) + (A.3.3), C1-1978:I.A + (K.1.44) + (A.3.3), C1-1979: I.A + (K.1.45) + (A.3.3), C1-1980:I.A + (K.1.47) + (A.3.3), C1-1981: I.A + (K.1.49) + (A.3.3), C1-1982:I.A + (K.1.53) + (A.3.3), C1-1983: I.A + (K.1.54) + (A.3.3), C1-1984:I.A + (A.1.4) + (A.3.4), C1- 1985: I.A + (A.1.12) + (A.3.4), C1-1986:I.A + (A.1.21) + (A.3.4), C1-1987: I.A + (A.1,21a) + (A.3.4), C1-1988:I.A + (A.1.24) + (A.3.4), C1-1989: I.A + (A.1.26) + (A.3.4), C1-1990:I.A + (A.1.27) + (A.3.4), C1-1991: I.A + (A.1.30) + (A.3.4), C1-1992:I.A + (A.1.31) + (A.3.4), C1-1993: I.A + (A.1.32) + (A.3.4), C1-1994:I.A + (A.1.35) + (A.3.4), C1-1995: I.A + (A.2.1) + (A.3.4), C1- 1996:I.A + (A.2.3) + (A.3.4), C1-1997: I.A + (A.2.5) + (A.3.4), C1-1998:I.A + (A.3.7) + (A.3.4), C1-1999: I.A + (A.3.9) + (A.3.4), C1-2000:I.A + (A.3.11) + (A.3.4), C1-2001: I.A + (A.3.12) + (A.3.4), C1-2002:I.A + (A.3.15) + (A.3.4), C1-2003: I.A + (A.3.16) + (A.3.4), C1-2004:I.A + (A.3.17) + (A.3.4), C1-2005: I.A + (A.3.18) + (A.3.4), C1-2006:I.A + (A.3.19) + (A.3.4), C1-2007: I.A + (A.3.20) + (A.3.4), C1-2008:I.A + (A.3.21) + (A.3.4), C1-2009: I.A + (A.3.22) + (A.3.4), C1- 2010:I.A + (A.3.23) + (A.3.4), C1-2011: I.A + (A.3.24) + (A.3.4), C1-2012:I.A + (A.3.25) + (A.3.4), C1-2013: I.A + (A.3.26) + (A.3.4), C1-2014:I.A + (A.3.27) + (A.3.4), C1-2015: I.A + (A.3.28) + (A.3.4), C1-2016:I.A + (A.3.29) + (A.3.4), C1-2017: I.A + (A.3.31) + (A.3.4), C1-2018:I.A + (A.3.32) + (A.3.4), C1-2019: I.A + (A.3.33) + (A.3.4), C1-2020:I.A + (A.3.34) + (A.3.4), C1- 2021: I.A + (A.3.35) + (A.3.4), C1-2022:I.A + (A.3.36) + (A.3.4), C1-2023: I.A + (A.3.37) + (A.3.4), C1-2024:I.A + (A.3.38) + (A.3.4), C1-2025: I.A + (A.3.39) + (A.3.4), C1-2026:I.A + (A.4.5) + (A.3.4), C1-2027: I.A + (A.4.11) + (A.3.4), C1-2028:I.A + (B.1.4) + (A.3.4), C1-2029: I.A + (B.1.5) + (A.3.4), C1-2030:I.A + (B.1.8.) + (A.3.4), C1-2031: I.A + (B.1.10) + (A.3.4), C1- 2032:I.A + (B.1.11) + (A.3.4), C1-2033: I.A + (B.1.12) + (A.3.4), C1-2034:I.A + (B.1.13) + (A.3.4), C1-2035: I.A + (B.1.17) + (A.3.4), C1-2036:I.A + (B.1.18) + (A.3.4), C1-2037: I.A + (B.1.21) + (A.3.4), C1-2038:I.A + (B.1.22) + (A.3.4), C1-2039: I.A + (B.1.23) + (A.3.4), C1-2040:I.A + (B.1.25) + (A.3.4), C1-2041: I.A + (B.1.26) + (A.3.4), C1-2042:I.A + (B.1.29) + (A.3.4), C1- 2043: I.A + (B.1.33) + (A.3.4), C1-2044:I.A + (B.1.34) + (A.3.4), C1-2045: I.A + (B.1.37) + (A.3.4), C1-2046:I.A + (B.1.38) + (A.3.4), C1-2047: I.A + (B.1.43) + (A.3.4), C1-2048:I.A + (B.1.46) + (A.3.4), C1-2049: I.A + (B.2.4) + (A.3.4), C1-2050:I.A + (B.2.5) + (A.3.4), C1-2051: I.A + (B.2.6) + (A.3.4), C1-2052:I.A + (B.2.8) + (A.3.4), C1-2053: I.A + (C.1.1) + (A.3.4), C1- 2054:I.A + (C.1.2) + (A.3.4), C1-2055: I.A + (C.1.4) + (A.3.4), C1-2056:I.A + (C.1.5) + (A.3.4), C1-2057: I.A + (C.2.6) + (A.3.4), C1-2058:I.A + (C.2.7) + (A.3.4), C1-2059: I.A + (C.2.8) + (A.3.4), C1-2060:I.A + (D.1.1) + (A.3.4), C1-2061: I.A + (D.1.2) + (A.3.4), C1-2062:I.A + (D.1.5) + (A.3.4), C1-2063: I.A + (D.2.4) + (A.3.4), C1-2064:I.A + (D.2.6) + (A.3.4), C1-2065: I.A + (D.2.7) + (A.3.4), C1-2066:I.A + (E.1.1) + (A.3.4), C1-2067: I.A + (E.1.3) + (A.3.4), C1-2068:I.A + (E.2.2) + (A.3.4), C1-2069: I.A + (E.2.3) + (A.3.4), C1-2070:I.A + (F.1.2) + (A.3.4), C1-2071: I.A + (F.1.4) + (A.3.4), C1-2072:I.A + (F.1.5) + (A.3.4), C1-2073: I.A + (G.3.1) + (A.3.4), C1- 2074:I.A + (G.3.3) + (A.3.4), C1-2075: I.A + (G.3.6) + (A.3.4), C1-2076:I.A + (G.5.1) + (A.3.4), C1-2077: I.A + (G.5.2) + (A.3.4), C1-2078:I.A + (G.5.3) + (A.3.4), C1-2079: I.A + (G.5.4) + (A.3.4), C1-2080:I.A + (G.5.5) + (A.3.4), C1-2081: I.A + (G.5.6) + (A.3.4), C1-2082:I.A + (G.5.7) + (A.3.4), C1-2083: I.A + (G.5.8) + (A.3.4), C1-2084:I.A + (G.5.9) + (A.3.4), C1-2085: I.A + (G.5.10) + (A.3.4), C1-2086:I.A + (G.5.11) + (A.3.4), C1-2087: I.A + (H.1.5) + (A.3.4), C1- 2088:I.A + (H.1.7) + (A.3.4), C1-2089: I.A + (H.2.2) + (A.3.4), C1-2090:I.A + (H.2.3) + (A.3.4), C1-2091: I.A + (H.2.5) + (A.3.4), C1-2092:I.A + (H.2.7) + (A.3.4), C1-2093: I.A + (H.2.8) + (A.3.4), C1-2094:I.A + (H.3.2) + (A.3.4), C1-2095: I.A + (H.3.4) + (A.3.4), C1-2096:I.A + (H.3.5) + (A.3.4), C1-2097: I.A + (H.4.9) + (A.3.4), C1-2098:I.A + (H.4.10) + (A.3.4), C1-2099: I.A + (I.2.2) + (A.3.4), C1-2100:I.A + (I.2.5) + (A.3.4), C1-2101: I.A + (J.1.2) + (A.3.4), C1-2102:I.A + (J.1.5) + (A.3.4), C1-2103: I.A + (J.1.8) + (A.3.4), C1-2104:I.A + (J.1.11) + (A.3.4), C1-2105: I.A + (J.1.12) + (A.3.4), C1-2106:I.A + (K.1.3) + (A.3.4), C1-2107: I.A + (K.1.29) + (A.3.4), C1- 2108:I.A + (K.1.30) + (A.3.4), C1-2109: I.A + (K.1.31) + (A.3.4), C1-2110:I.A + (K.1.32) + (A.3.4), C1-2111: I.A + (K.1.41) + (A.3.4), C1-2112:I.A + (K.1.42) + (A.3.4), C1-2113: I.A + (K.1.44) + (A.3.4), C1-2114:I.A + (K.1.45) + (A.3.4), C1-2115: I.A + (K.1.47) + (A.3.4), C1-2116:I.A + (K.1.49) + (A.3.4), C1-2117: I.A + (K.1.53) + (A.3.4), C1-2118:I.A + (K.1.54) + (A.3.4), C1- 2119: I.A + (A.1.4) + (A.3.7), C1-2120:I.A + (A.1.12) + (A.3.7), C1-2121: I.A + (A.1.21) + (A.3.7), C1-2122:I.A + (A.1,21a) + (A.3.7), C1-2123: I.A + (A.1.24) + (A.3.7), C1-2124:I.A + (A.1.26) + (A.3.7), C1-2125: I.A + (A.1.27) + (A.3.7), C1-2126:I.A + (A.1.30) + (A.3.7), C1-2127: I.A + (A.1.31) + (A.3.7), C1-2128:I.A + (A.1.32) + (A.3.7), C1-2129: I.A + (A.1.35) + (A.3.7), C1- 2130:I.A + (A.2.1) + (A.3.7), C1-2131: I.A + (A.2.3) + (A.3.7), C1-2132:I.A + (A.2.5) + (A.3.7), C1-2133: I.A + (A.3.9) + (A.3.7), C1-2134:I.A + (A.3.11) + (A.3.7), C1-2135: I.A + (A.3.12) + (A.3.7), C1-2136:I.A + (A.3.15) + (A.3.7), C1-2137: I.A + (A.3.16) + (A.3.7), C1-2138:I.A + (A.3.17) + (A.3.7), C1-2139: I.A + (A.3.18) + (A.3.7), C1-2140:I.A + (A.3.19) + (A.3.7), C1-2141: I.A + (A.3.20) + (A.3.7), C1-2142:I.A + (A.3.21) + (A.3.7), C1-2143: I.A + (A.3.22) + (A.3.7), C1- 2144:I.A + (A.3.23) + (A.3.7), C1-2145: I.A + (A.3.24) + (A.3.7), C1-2146:I.A + (A.3.25) + (A.3.7), C1-2147: I.A + (A.3.26) + (A.3.7), C1-2148:I.A + (A.3.27) + (A.3.7), C1-2149: I.A + (A.3.28) + (A.3.7), C1-2150:I.A + (A.3.29) + (A.3.7), C1-2151: I.A + (A.3.31) + (A.3.7), C1-2152:I.A + (A.3.32) + (A.3.7), C1-2153: I.A + (A.3.33) + (A.3.7), C1-2154:I.A + (A.3.34) + (A.3.7), C1- 2155: I.A + (A.3.35) + (A.3.7), C1-2156:I.A + (A.3.36) + (A.3.7), C1-2157: I.A + (A.3.37) + (A.3.7), C1-2158:I.A + (A.3.38) + (A.3.7), C1-2159: I.A + (A.3.39) + (A.3.7), C1-2160:I.A + (A.4.5) + (A.3.7), C1-2161: I.A + (A.4.11) + (A.3.7), C1-2162:I.A + (B.1.4) + (A.3.7), C1-2163: I.A + (B.1.5) + (A.3.7), C1-2164:I.A + (B.1.8.) + (A.3.7), C1-2165: I.A + (B.1.10) + (A.3.7), C1- 2166:I.A + (B.1.11) + (A.3.7), C1-2167: I.A + (B.1.12) + (A.3.7), C1-2168:I.A + (B.1.13) + (A.3.7), C1-2169: I.A + (B.1.17) + (A.3.7), C1-2170:I.A + (B.1.18) + (A.3.7), C1-2171: I.A + (B.1.21) + (A.3.7), C1-2172:I.A + (B.1.22) + (A.3.7), C1-2173: I.A + (B.1.23) + (A.3.7), C1-2174:I.A + (B.1.25) + (A.3.7), C1-2175: I.A + (B.1.26) + (A.3.7), C1-2176:I.A + (B.1.29) + (A.3.7), C1- 2177: I.A + (B.1.33) + (A.3.7), C1-2178:I.A + (B.1.34) + (A.3.7), C1-2179: I.A + (B.1.37) + (A.3.7), C1-2180:I.A + (B.1.38) + (A.3.7), C1-2181: I.A + (B.1.43) + (A.3.7), C1-2182:I.A + (B.1.46) + (A.3.7), C1-2183: I.A + (B.2.4) + (A.3.7), C1-2184:I.A + (B.2.5) + (A.3.7), C1-2185: I.A + (B.2.6) + (A.3.7), C1-2186:I.A + (B.2.8) + (A.3.7), C1-2187: I.A + (C.1.1) + (A.3.7), C1- 2188:I.A + (C.1.2) + (A.3.7), C1-2189: I.A + (C.1.4) + (A.3.7), C1-2190:I.A + (C.1.5) + (A.3.7), C1-2191: I.A + (C.2.6) + (A.3.7), C1-2192:I.A + (C.2.7) + (A.3.7), C1-2193: I.A + (C.2.8) + (A.3.7), C1-2194:I.A + (D.1.1) + (A.3.7), C1-2195: I.A + (D.1.2) + (A.3.7), C1-2196:I.A + (D.1.5) + (A.3.7), C1-2197: I.A + (D.2.4) + (A.3.7), C1-2198:I.A + (D.2.6) + (A.3.7), C1-2199: I.A + (D.2.7) + (A.3.7), C1-2200:I.A + (E.1.1) + (A.3.7), C1-2201: I.A + (E.1.3) + (A.3.7), C1-2202:I.A + (E.2.2) + (A.3.7), C1-2203: I.A + (E.2.3) + (A.3.7), C1-2204:I.A + (F.1.2) + (A.3.7), C1-2205: I.A + (F.1.4) + (A.3.7), C1-2206:I.A + (F.1.5) + (A.3.7), C1-2207: I.A + (G.3.1) + (A.3.7), C1- 2208:I.A + (G.3.3) + (A.3.7), C1-2209: I.A + (G.3.6) + (A.3.7), C1-2210:I.A + (G.5.1) + (A.3.7), C1-2211: I.A + (G.5.2) + (A.3.7), C1-2212:I.A + (G.5.3) + (A.3.7), C1-2213: I.A + (G.5.4) + (A.3.7), C1-2214:I.A + (G.5.5) + (A.3.7), C1-2215: I.A + (G.5.6) + (A.3.7), C1-2216:I.A + (G.5.7) + (A.3.7), C1-2217: I.A + (G.5.8) + (A.3.7), C1-2218:I.A + (G.5.9) + (A.3.7), C1-2219: I.A + (G.5.10) + (A.3.7), C1-2220:I.A + (G.5.11) + (A.3.7), C1-2221: I.A + (H.1.5) + (A.3.7), C1- 2222:I.A + (H.1.7) + (A.3.7), C1-2223: I.A + (H.2.2) + (A.3.7), C1-2224:I.A + (H.2.3) + (A.3.7), C1-2225: I.A + (H.2.5) + (A.3.7), C1-2226:I.A + (H.2.7) + (A.3.7), C1-2227: I.A + (H.2.8) + (A.3.7), C1-2228:I.A + (H.3.2) + 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C1-2375: I.A + (K.1.30) + (A.3.9), C1- 2376:I.A + (K.1.31) + (A.3.9), C1-2377: I.A + (K.1.32) + (A.3.9), C1-2378:I.A + (K.1.41) + (A.3.9), C1-2379: I.A + (K.1.42) + (A.3.9), C1-2380:I.A + (K.1.44) + (A.3.9), C1-2381: I.A + (K.1.45) + (A.3.9), C1-2382:I.A + (K.1.47) + (A.3.9), C1-2383: I.A + (K.1.49) + (A.3.9), C1-2384:I.A + (K.1.53) + (A.3.9), C1-2385: I.A + (K.1.54) + (A.3.9), C1-2386:I.A + (A.1.4) + (A.3.17), C1- 2387: I.A + (A.1.12) + (A.3.17), C1-2388:I.A + (A.1.21) + (A.3.17), C1-2389: I.A + (A.1,21a) + (A.3.17), C1-2390:I.A + (A.1.24) + (A.3.17), C1-2391: I.A + (A.1.26) + (A.3.17), C1-2392:I.A + (A.1.27) + (A.3.17), C1-2393: I.A + (A.1.30) + (A.3.17), C1-2394:I.A + (A.1.31) + (A.3.17), C1- 2395: I.A + (A.1.32) + (A.3.17), C1-2396:I.A + (A.1.35) + (A.3.17), C1-2397: I.A + (A.2.1) + (A.3.17), C1-2398:I.A + (A.2.3) + (A.3.17), C1-2399: I.A + (A.2.5) + (A.3.17), C1-2400:I.A + (A.3.11) + (A.3.17), C1-2401: I.A + (A.3.12) + (A.3.17), C1-2402:I.A + (A.3.15) + (A.3.17), C1- 2403: I.A + 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(A.3.17), C1-2460:I.A + (D.1.2) + (A.3.17), C1-2461: I.A + (D.1.5) + (A.3.17), C1- 2462:I.A + (D.2.4) + (A.3.17), C1-2463: I.A + (D.2.6) + (A.3.17), C1-2464:I.A + (D.2.7) + (A.3.17), C1-2465: I.A + (E.1.1) + (A.3.17), C1-2466:I.A + (E.1.3) + (A.3.17), C1-2467: I.A + (E.2.2) + (A.3.17), C1-2468:I.A + (E.2.3) + (A.3.17), C1-2469: I.A + (F.1.2) + (A.3.17), C1-2470:I.A + (F.1.4) + (A.3.17), C1-2471: I.A + (F.1.5) + (A.3.17), C1-2472:I.A + (G.3.1) + (A.3.17), C1- 2473: I.A + (G.3.3) + (A.3.17), C1-2474:I.A + (G.3.6) + (A.3.17), C1-2475: I.A + (G.5.1) + (A.3.17), C1-2476:I.A + (G.5.2) + (A.3.17), C1-2477: I.A + (G.5.3) + (A.3.17), C1-2478:I.A + (G.5.4) + (A.3.17), C1-2479: I.A + (G.5.5) + (A.3.17), C1-2480:I.A + (G.5.6) + (A.3.17), C1- 2481: I.A + (G.5.7) + (A.3.17), C1-2482:I.A + (G.5.8) + (A.3.17), C1-2483: I.A + (G.5.9) + (A.3.17), C1-2484:I.A + (G.5.10) + (A.3.17), C1-2485: I.A + (G.5.11) + (A.3.17), C1-2486:I.A + (H.1.5) + (A.3.17), C1-2487: I.A + (H.1.7) + (A.3.17), C1-2488:I.A + 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(B.2.8) + (B.1.4), C1-4077: I.A + (C.1.1) +(B.1.4), C1-4078: I.A + (C.1.2) + (B.1.4), C1-4079: I.A + (C.1.4) +(B.1.4), C1-4080: I.A + (C.1.5) + (B.1.4), C1-4081: I.A + (C.2.6) +(B.1.4), C1-4082: I.A + (C.2.7) + (B.1.4), C1-4083: I.A + (C.2.8) +(B.1.4), C1-4084: I.A + (D.1.1) + (B.1.4), C1-4085: I.A + (D.1.2) +(B.1.4), C1-4086: I.A + (D.1.5) + (B.1.4), C1-4087: I.A + (D.2.4) +(B.1.4), C1-4088: I.A + (D.2.6) + (B.1.4), C1-4089: I.A + (D.2.7) +(B.1.4), C1-4090: I.A + (E.1.1) + (B.1.4), C1-4091: I.A + (E.1.3) +(B.1.4), C1- 4092: I.A + (E.2.2) + (B.1.4), C1-4093: I.A + (E.2.3) +(B.1.4), C1-4094: I.A + (F.1.2) + (B.1.4), C1-4095: I.A + (F.1.4) +(B.1.4), C1-4096: I.A + (F.1.5) + (B.1.4), C1-4097: I.A + (G.3.1) +(B.1.4), C1-4098: I.A + (G.3.3) + (B.1.4), C1-4099: I.A + (G.3.6) +(B.1.4), C1-4100: I.A + (G.5.1) + (B.1.4), C1-4101: I.A + (G.5.2) +(B.1.4), C1-4102: I.A + (G.5.3) + (B.1.4), C1-4103: I.A + (G.5.4) +(B.1.4), C1-4104: I.A + (G.5.5) + (B.1.4), C1-4105: I.A + (G.5.6) +(B.1.4), C1- 4106: I.A + (G.5.7) + (B.1.4), C1-4107: I.A + (G.5.8) +(B.1.4), C1-4108: I.A + (G.5.9) + (B.1.4), C1-4109: I.A + (G.5.10) +(B.1.4), C1-4110: I.A + (G.5.11) + (B.1.4), C1-4111: I.A + (H.1.5) +(B.1.4), C1-4112: I.A + (H.1.7) + (B.1.4), C1-4113: I.A + (H.2.2) +(B.1.4), C1-4114: I.A + (H.2.3) + (B.1.4), C1-4115: I.A + (H.2.5) +(B.1.4), C1-4116: I.A + (H.2.7) + (B.1.4), C1-4117: I.A + (H.2.8) +(B.1.4), C1-4118: I.A + (H.3.2) + (B.1.4), C1-4119: I.A + (H.3.4) +(B.1.4), C1-4120: I.A + (H.3.5) + (B.1.4), C1-4121: I.A + (H.4.9) +(B.1.4), C1-4122: I.A + (H.4.10) + (B.1.4), C1-4123: I.A + (I.2.2) +(B.1.4), C1-4124: I.A + (I.2.5) + (B.1.4), C1-4125: I.A + (J.1.2) +(B.1.4), C1-4126: I.A + (J.1.5) + (B.1.4), C1-4127: I.A + (J.1.8) +(B.1.4), C1-4128: I.A + (J.1.11) + (B.1.4), C1- 4129: I.A + (J.1.12) +(B.1.4), C1-4130: I.A + (K.1.3) + (B.1.4), C1-4131: I.A + (K.1.29) +(B.1.4), C1-4132: I.A + (K.1.30) + (B.1.4), C1-4133: I.A + (K.1.31) +(B.1.4), C1-4134: I.A + (K.1.32) + (B.1.4), C1-4135: I.A + (K.1.41) +(B.1.4), C1-4136: I.A + (K.1.42) + (B.1.4), C1-4137: I.A + (K.1.44) +(B.1.4), C1-4138: I.A + (K.1.45) + (B.1.4), C1-4139: I.A + (K.1.47) +(B.1.4), C1-4140: I.A + (K.1.49) + (B.1.4), C1-4141: I.A + (K.1.53) +(B.1.4), C1-4142: I.A + (K.1.54) + (B.1.4), C1- 4143: I.A + (A.1.4) +(B.1.5), C1-4144: I.A + (A.1.12) + (B.1.5), C1-4145: I.A + (A.1.21) +(B.1.5), C1-4146: I.A + (A.1,21a) + (B.1.5), C1-4147: I.A + (A.1.24) +(B.1.5), C1-4148: I.A + (A.1.26) + (B.1.5), C1-4149: I.A + (A.1.27) +(B.1.5), C1-4150: I.A + (A.1.30) + (B.1.5), C1-4151: I.A + (A.1.31) +(B.1.5), C1-4152: I.A + (A.1.32) + (B.1.5), C1-4153: I.A + (A.1.35) +(B.1.5), C1- 4154: I.A + (A.2.1) + (B.1.5), C1-4155: I.A + (A.2.3) +(B.1.5), C1-4156: I.A + (A.2.5) + (B.1.5), C1-4157: I.A + (A.3.11) +(B.1.5), C1-4158: I.A + (A.3.12) + (B.1.5), C1-4159: I.A + (A.3.15) +(B.1.5), C1-4160: I.A + (A.3.16) + (B.1.5), C1-4161: I.A + (A.3.18) +(B.1.5), C1-4162: I.A + (A.3.19) + (B.1.5), C1-4163: I.A + (A.3.20) +(B.1.5), C1-4164: I.A + (A.3.21) + (B.1.5), C1-4165: I.A + (A.3.22) +(B.1.5), C1-4166: I.A + (A.3.23) + (B.1.5), C1-4167: I.A + (A.3.25) +(B.1.5), C1- 4168: I.A + (A.3.26) + (B.1.5), C1-4169: I.A + (A.3.27) +(B.1.5), C1-4170: I.A + (A.4.5) + (B.1.5), C1-4171: I.A + (A.4.11) +(B.1.5), C1-4172: I.A + (B.1.8.) + (B.1.5), C1-4173: I.A + (B.1.10) +(B.1.5), C1-4174: I.A + (B.1.11) + (B.1.5), C1-4175: I.A + (B.1.12) +(B.1.5), C1-4176: I.A + (B.1.13) + (B.1.5), C1-4177: I.A + (B.1.17) +(B.1.5), C1-4178: I.A + (B.1.18) + (B.1.5), C1- 4179: I.A + (B.1.21) +(B.1.5), C1-4180: I.A + (B.1.22) + (B.1.5), C1-4181: I.A + (B.1.23) +(B.1.5), C1-4182: I.A + (B.1.25) + (B.1.5), C1-4183: I.A + (B.1.26) +(B.1.5), C1-4184: I.A + (B.1.29) + (B.1.5), C1-4185: I.A + (B.1.33) +(B.1.5), C1-4186: I.A + (B.1.34) + (B.1.5), C1-4187: I.A + (B.1.37) +(B.1.5), C1-4188: I.A + (B.1.38) + (B.1.5), C1-4189: I.A + (B.1.43) +(B.1.5), C1- 4190: I.A + (B.1.46) + (B.1.5), C1-4191: I.A + (B.2.4) +(B.1.5), C1-4192: I.A + (B.2.5) + (B.1.5), C1-4193: I.A + (B.2.6) +(B.1.5), C1-4194: I.A + (B.2.8) + (B.1.5), C1-4195: I.A + (C.1.1) +(B.1.5), C1-4196: I.A + (C.1.2) + (B.1.5), C1-4197: I.A + (C.1.4) +(B.1.5), C1-4198: I.A + (C.1.5) + (B.1.5), C1-4199: I.A + (C.2.6) +(B.1.5), C1-4200: I.A + (C.2.7) + (B.1.5), C1-4201: I.A + (C.2.8) +(B.1.5), C1-4202: I.A + (D.1.1) + (B.1.5), C1-4203: I.A + (D.1.2) +(B.1.5), C1-4204: I.A + (D.1.5) + (B.1.5), C1-4205: I.A + (D.2.4) +(B.1.5), C1-4206: I.A + (D.2.6) + (B.1.5), C1-4207: I.A + (D.2.7) +(B.1.5), C1-4208: I.A + (E.1.1) + (B.1.5), C1-4209: I.A + (E.1.3) +(B.1.5), C1- 4210: I.A + (E.2.2) + (B.1.5), C1-4211: I.A + (E.2.3) +(B.1.5), C1-4212: I.A + (F.1.2) + (B.1.5), C1-4213: I.A + (F.1.4) +(B.1.5), C1-4214: I.A + (F.1.5) + (B.1.5), C1-4215: I.A + (G.3.1) +(B.1.5), C1-4216: I.A + (G.3.3) + (B.1.5), C1-4217: I.A + (G.3.6) +(B.1.5), C1-4218: I.A + (G.5.1) + (B.1.5), C1-4219: I.A + (G.5.2) +(B.1.5), C1-4220: I.A + (G.5.3) + (B.1.5), C1-4221: I.A + (G.5.4) +(B.1.5), C1-4222: I.A + (G.5.5) + (B.1.5), C1-4223: I.A + (G.5.6) +(B.1.5), C1- 4224: I.A + (G.5.7) + (B.1.5), C1-4225: I.A + (G.5.8) +(B.1.5), C1-4226: I.A + (G.5.9) + (B.1.5), C1-4227: I.A + (G.5.10) +(B.1.5), C1-4228: I.A + (G.5.11) + (B.1.5), C1-4229: I.A + (H.1.5) +(B.1.5), C1-4230: I.A + (H.1.7) + (B.1.5), C1-4231: I.A + (H.2.2) +(B.1.5), C1-4232: I.A + (H.2.3) + (B.1.5), C1-4233: I.A + (H.2.5) +(B.1.5), C1-4234: I.A + (H.2.7) + (B.1.5), C1-4235: I.A + (H.2.8) +(B.1.5), C1-4236: I.A + (H.3.2) + (B.1.5), C1-4237: I.A + (H.3.4) +(B.1.5), C1-4238: I.A + (H.3.5) + (B.1.5), C1-4239: I.A + (H.4.9) +(B.1.5), C1-4240: I.A + (H.4.10) + (B.1.5), C1-4241: I.A + (I.2.2) +(B.1.5), C1-4242: I.A + (I.2.5) + (B.1.5), C1-4243: I.A + (J.1.2) +(B.1.5), C1-4244: I.A + (J.1.5) + (B.1.5), C1-4245: I.A + (J.1.8) +(B.1.5), C1-4246: I.A + (J.1.11) + (B.1.5), C1- 4247: I.A + (J.1.12) +(B.1.5), C1-4248: I.A + (K.1.3) + (B.1.5), C1-4249: I.A + (K.1.29) +(B.1.5), C1-4250: I.A + (K.1.30) + (B.1.5), C1-4251: I.A + (K.1.31) +(B.1.5), C1-4252: I.A + (K.1.32) + (B.1.5), C1-4253: I.A + (K.1.41) +(B.1.5), C1-4254: I.A + (K.1.42) + (B.1.5), C1-4255: I.A + (K.1.44) +(B.1.5), C1-4256: I.A + (K.1.45) + (B.1.5), C1-4257: I.A + (K.1.47) +(B.1.5), C1-4258: I.A + (K.1.49) + (B.1.5), C1-4259: I.A + (K.1.53) +(B.1.5), C1-4260: I.A + (K.1.54) + (B.1.5), C1- 4261: I.A + (A.1.4) +(B.1.8), C1-4262: I.A + (A.1.12) + (B.1.8), C1-4263: I.A + (A.1.21) +(B.1.8), C1-4264: I.A + (A.1,21a) + (B.1.8), C1-4265: I.A + (A.1.24) +(B.1.8), C1-4266: I.A + (A.1.26) + (B.1.8), C1-4267: I.A + (A.1.27) +(B.1.8), C1-4268: I.A + (A.1.30) + (B.1.8), C1-4269: I.A + (A.1.31) +(B.1.8), C1-4270: I.A + (A.1.32) + (B.1.8), C1-4271: I.A + (A.1.35) +(B.1.8), C1- 4272: I.A + (A.2.1) + (B.1.8), C1-4273: I.A + (A.2.3) +(B.1.8), C1-4274: I.A + (A.2.5) + (B.1.8), C1-4275: I.A + (A.3.11) +(B.1.8), C1-4276: I.A + (A.3.12) + (B.1.8), C1-4277: I.A + (A.3.15) +(B.1.8), C1-4278: I.A + (A.3.16) + (B.1.8), C1-4279: I.A + (A.3.18) +(B.1.8), C1-4280: I.A + (A.3.19) + (B.1.8), C1-4281: I.A + (A.3.20) +(B.1.8), 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C1-4311: I.A + (B.2.8) +(B.1.8), C1-4312: I.A + (C.1.1) + (B.1.8), C1-4313: I.A + (C.1.2) +(B.1.8), C1-4314: I.A + (C.1.4) + (B.1.8), C1-4315: I.A + (C.1.5) +(B.1.8), C1-4316: I.A + (C.2.6) + (B.1.8), C1-4317: I.A + (C.2.7) +(B.1.8), C1-4318: I.A + (C.2.8) + (B.1.8), C1-4319: I.A + (D.1.1) +(B.1.8), C1-4320: I.A + (D.1.2) + (B.1.8), C1-4321: I.A + (D.1.5) +(B.1.8), C1-4322: I.A + (D.2.4) + (B.1.8), C1-4323: I.A + (D.2.6) +(B.1.8), C1-4324: I.A + (D.2.7) + (B.1.8), C1-4325: I.A + (E.1.1) +(B.1.8), C1-4326: I.A + (E.1.3) + (B.1.8), C1-4327: I.A + (E.2.2) +(B.1.8), C1- 4328: I.A + (E.2.3) + (B.1.8), C1-4329: I.A + (F.1.2) +(B.1.8), C1-4330: I.A + (F.1.4) + (B.1.8), C1-4331: I.A + (F.1.5) +(B.1.8), C1-4332: I.A + (G.3.1) + (B.1.8), C1-4333: I.A + (G.3.3) +(B.1.8), C1-4334: I.A + (G.3.6) + (B.1.8), C1-4335: I.A + (G.5.1) +(B.1.8), C1-4336: I.A + (G.5.2) + (B.1.8), C1-4337: I.A + (G.5.3) +(B.1.8), C1-4338: I.A + (G.5.4) + (B.1.8), C1-4339: I.A + (G.5.5) +(B.1.8), C1-4340: I.A + (G.5.6) + 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I.A + (D.1.1) + (B.2.4), C1-5111: I.A +(D.1.2) + (B.2.4), C1-5112: I.A + (D.1.5) + (B.2.4), C1-5113: I.A +(D.2.4) + (B.2.4), C1-5114: I.A + (D.2.6) + (B.2.4), C1-5115: I.A +(D.2.7) + (B.2.4), C1-5116: I.A + (E.1.1) + (B.2.4), C1-5117: I.A +(E.1.3) + (B.2.4), C1-5118: I.A + (E.2.2) + (B.2.4), C1-5119: I.A +(E.2.3) + (B.2.4), C1-5120: I.A + (F.1.2) + (B.2.4), C1-5121: I.A +(F.1.4) + (B.2.4), C1-5122: I.A + (F.1.5) + (B.2.4), C1-5123: I.A +(G.3.1) + (B.2.4), C1-5124: I.A + (G.3.3) + (B.2.4), C1-5125: I.A +(G.3.6) + (B.2.4), C1-5126: I.A + (G.5.1) + (B.2.4), C1-5127: I.A +(G.5.2) + (B.2.4), C1-5128: I.A + (G.5.3) + (B.2.4), C1- 5129: I.A +(G.5.4) + (B.2.4), C1-5130: I.A + (G.5.5) + (B.2.4), C1-5131: I.A +(G.5.6) + (B.2.4), C1-5132: I.A + (G.5.7) + (B.2.4), C1-5133: I.A +(G.5.8) + (B.2.4), C1-5134: I.A + (G.5.9) + (B.2.4), C1-5135: I.A +(G.5.10) + (B.2.4), C1-5136: I.A + (G.5.11) + (B.2.4), C1-5137: I.A +(H.1.5) + (B.2.4), C1-5138: I.A + (H.1.7) + (B.2.4), C1-5139: I.A +(H.2.2) + (B.2.4), C1-5140: I.A + (H.2.3) + (B.2.4), C1-5141: I.A +(H.2.5) + (B.2.4), C1-5142: I.A + (H.2.7) + (B.2.4), C1-5143: I.A +(H.2.8) + (B.2.4), C1-5144: I.A + (H.3.2) + (B.2.4), C1-5145: I.A +(H.3.4) + (B.2.4), C1- 5146: I.A + (H.3.5) + (B.2.4), C1-5147: I.A +(H.4.9) + (B.2.4), C1-5148: I.A + (H.4.10) + (B.2.4), C1-5149: I.A +(I.2.2) + (B.2.4), C1-5150: I.A + (I.2.5) + (B.2.4), C1-5151: I.A +(J.1.2) + (B.2.4), C1-5152: I.A + (J.1.5) + (B.2.4), C1-5153: I.A +(J.1.8) + (B.2.4), C1-5154: I.A + (J.1.11) + (B.2.4), C1-5155: I.A +(J.1.12) + (B.2.4), C1-5156: I.A + (K.1.3) + (B.2.4), C1-5157: I.A +(K.1.29) + (B.2.4), C1-5158: I.A + (K.1.30) + (B.2.4), C1-5159: I.A +(K.1.31) + (B.2.4), C1-5160: I.A + (K.1.32) + (B.2.4), C1-5161: I.A +(K.1.41) + (B.2.4), C1-5162: I.A + (K.1.42) + (B.2.4), C1- 5163: I.A +(K.1.44) + (B.2.4), C1-5164: I.A + (K.1.45) + (B.2.4), C1-5165: I.A +(K.1.47) + (B.2.4), C1-5166: I.A + (K.1.49) + (B.2.4), C1-5167: I.A +(K.1.53) + (B.2.4), C1-5168: I.A + (K.1.54) + (B.2.4), C1-5169: I.A +(A.1.4) + (B.2.6), C1-5170: I.A + (A.1.12) + (B.2.6), C1-5171: I.A +(A.1.21) + (B.2.6), C1-5172: I.A + (A.1,21a) + (B.2.6), C1-5173: I.A +(A.1.24) + (B.2.6), C1-5174: I.A + (A.1.26) + (B.2.6), C1-5175: I.A +(A.1.27) + (B.2.6), C1-5176: I.A + (A.1.30) + (B.2.6), C1-5177: I.A +(A.1.31) + (B.2.6), C1-5178: I.A + (A.1.32) + (B.2.6), C1-5179: I.A +(A.1.35) + (B.2.6), C1-5180: I.A + (A.2.1) + (B.2.6), C1-5181: I.A +(A.2.3) + (B.2.6), C1-5182: I.A + (A.2.5) + (B.2.6), C1-5183: I.A +(A.3.11) + (B.2.6), C1-5184: I.A + (A.3.12) + (B.2.6), C1- 5185: I.A +(A.3.15) + (B.2.6), C1-5186: I.A + (A.3.16) + (B.2.6), C1-5187: I.A +(A.3.18) + (B.2.6), C1-5188: I.A + (A.3.19) + (B.2.6), C1-5189: I.A +(A.3.20) + (B.2.6), C1-5190: I.A + (A.3.21) + (B.2.6), C1-5191: I.A +(A.3.22) + (B.2.6), C1-5192: I.A + (A.3.23) + (B.2.6), C1-5193: I.A +(A.3.25) + (B.2.6), C1-5194: I.A + (A.3.26) + (B.2.6), C1-5195: I.A +(A.3.27) + (B.2.6), C1- 5196: I.A + (A.4.5) + (B.2.6), C1-5197: I.A +(A.4.11) + (B.2.6), C1-5198: I.A + (B.1.10) + (B.2.6), C1-5199: I.A +(B.1.11) + (B.2.6), C1-5200: I.A + (B.1.12) + (B.2.6), C1-5201: I.A +(B.1.13) + (B.2.6), C1-5202: I.A + (B.1.18) + (B.2.6), C1-5203: I.A +(B.1.21) + (B.2.6), C1-5204: I.A + (B.1.26) + (B.2.6), C1-5205: I.A +(B.1.33) + (B.2.6), C1-5206: I.A + (B.1.34) + (B.2.6), C1- 5207: I.A +(B.1.37) + (B.2.6), C1-5208: I.A + (B.1.43) + (B.2.6), C1-5209: I.A +(B.1.46) + (B.2.6), C1-5210: I.A + (B.2.5) + (B.2.6), C1-5211: I.A +(B.2.8) + (B.2.6), C1-5212: I.A + (C.1.1) + (B.2.6), C1-5213: I.A +(C.1.2) + (B.2.6), C1-5214: I.A + (C.1.4) + (B.2.6), C1-5215: I.A +(C.1.5) + (B.2.6), C1-5216: I.A + (C.2.6) + (B.2.6), C1-5217: I.A +(C.2.7) + (B.2.6), C1-5218: I.A + (C.2.8) + (B.2.6), C1-5219: I.A +(D.1.1) + (B.2.6), C1-5220: I.A + (D.1.2) + (B.2.6), C1-5221: I.A +(D.1.5) + (B.2.6), C1-5222: I.A + (D.2.4) + (B.2.6), C1-5223: I.A +(D.2.6) + (B.2.6), C1- 5224: I.A + (D.2.7) + (B.2.6), C1-5225: I.A +(E.1.1) + (B.2.6), C1-5226: I.A + (E.1.3) + (B.2.6), C1-5227: I.A +(E.2.2) + (B.2.6), C1-5228: I.A + (E.2.3) + (B.2.6), C1-5229: I.A +(F.1.2) + (B.2.6), C1-5230: I.A + (F.1.4) + (B.2.6), C1-5231: I.A +(F.1.5) + (B.2.6), C1-5232: I.A + (G.3.1) + (B.2.6), C1-5233: I.A +(G.3.3) + (B.2.6), C1-5234: I.A + (G.3.6) + (B.2.6), C1-5235: I.A +(G.5.1) + (B.2.6), C1-5236: I.A + (G.5.2) + (B.2.6), C1-5237: I.A +(G.5.3) + (B.2.6), C1-5238: I.A + (G.5.4) + (B.2.6), C1-5239: I.A +(G.5.5) + (B.2.6), C1-5240: I.A + (G.5.6) + (B.2.6), C1- 5241: I.A +(G.5.7) + (B.2.6), C1-5242: I.A + (G.5.8) + (B.2.6), C1-5243: I.A +(G.5.9) + (B.2.6), C1-5244: I.A + (G.5.10) + (B.2.6), C1-5245: I.A +(G.5.11) + (B.2.6), C1-5246: I.A + (H.1.5) + (B.2.6), C1-5247: I.A +(H.1.7) + (B.2.6), C1-5248: I.A + (H.2.2) + (B.2.6), C1-5249: I.A +(H.2.3) + (B.2.6), C1-5250: I.A + (H.2.5) + (B.2.6), C1-5251: I.A +(H.2.7) + (B.2.6), C1-5252: I.A + (H.2.8) + (B.2.6), C1-5253: I.A +(H.3.2) + (B.2.6), C1-5254: I.A + (H.3.4) + (B.2.6), C1-5255: I.A +(H.3.5) + (B.2.6), C1-5256: I.A + (H.4.9) + (B.2.6), C1-5257: I.A +(H.4.10) + (B.2.6), C1-5258: I.A + (I.2.2) + (B.2.6), C1-5259: I.A +(I.2.5) + (B.2.6), C1-5260: I.A + (J.1.2) + (B.2.6), C1-5261: I.A +(J.1.5) + (B.2.6), C1-5262: I.A + (J.1.8) + (B.2.6), C1-5263: I.A +(J.1.11) + (B.2.6), C1- 5264: I.A + (J.1.12) + (B.2.6), C1-5265: I.A +(K.1.3) + (B.2.6), C1-5266: I.A + (K.1.29) + (B.2.6), C1-5267: I.A +(K.1.30) + (B.2.6), C1-5268: I.A + (K.1.31) + (B.2.6), C1-5269: I.A +(K.1.32) + (B.2.6), C1-5270: I.A + (K.1.41) + (B.2.6), C1-5271: I.A +(K.1.42) + (B.2.6), C1-5272: I.A + (K.1.44) + (B.2.6), C1-5273: I.A +(K.1.45) + (B.2.6), C1-5274: I.A + (K.1.47) + (B.2.6), C1-5275: I.A +(K.1.49) + (B.2.6), C1-5276: I.A + (K.1.53) + (B.2.6), C1-5277: I.A +(K.1.54) + (B.2.6), C1- 5278: I.A + (A.1.4) + (D.2.6), C1-5279: I.A +(A.1.12) + (D.2.6), C1-5280: I.A + (A.1.21) + (D.2.6), C1-5281: I.A +(A.1,21a) + (D.2.6), C1-5282: I.A + (A.1.24) + (D.2.6), C1-5283: I.A +(A.1.26) + (D.2.6), C1-5284: I.A + (A.1.27) + (D.2.6), C1-5285: I.A +(A.1.30) + (D.2.6), C1- 5286: I.A + (A.1.31) + (D.2.6), C1-5287: I.A +(A.1.32) + (D.2.6), C1-5288: I.A + (A.1.35) + (D.2.6), C1-5289: I.A +(A.2.1) + (D.2.6), C1-5290: I.A + (A.2.3) + (D.2.6), C1-5291: I.A +(A.2.5) + (D.2.6), C1-5292: I.A + (A.3.11) + (D.2.6), C1-5293: I.A +(A.3.12) + (D.2.6), C1-5294: I.A + (A.3.15) + (D.2.6), C1-5295: I.A +(A.3.16) + (D.2.6), C1-5296: I.A + (A.3.18) + (D.2.6), C1- 5297: I.A +(A.3.19) + (D.2.6), C1-5298: I.A + (A.3.20) + (D.2.6), C1-5299: I.A +(A.3.21) + (D.2.6), C1-5300: I.A + (A.3.22) + (D.2.6), C1-5301: I.A +(A.3.23) + (D.2.6), C1-5302: I.A + (A.3.25) + (D.2.6), C1-5303: I.A +(A.3.26) + (D.2.6), C1-5304: I.A + (A.3.27) + (D.2.6), C1- 5305: I.A +(A.4.5) + (D.2.6), C1-5306: I.A + (A.4.11) + (D.2.6), C1-5307: I.A +(B.1.10) + (D.2.6), C1-5308: I.A + (B.1.11) + (D.2.6), C1-5309: I.A +(B.1.12) + (D.2.6), C1-5310: I.A + (B.1.13) + (D.2.6), C1-5311: I.A +(B.1.18) + (D.2.6), C1-5312: I.A + (B.1.21) + (D.2.6), C1- 5313: I.A +(B.1.26) + (D.2.6), C1-5314: I.A + (B.1.33) + (D.2.6), C1-5315: I.A 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C1-5345: I.A +(G.5.3) + (D.2.6), C1-5346: I.A + (G.5.4) + (D.2.6), C1-5347: I.A +(G.5.5) + (D.2.6), C1-5348: I.A + (G.5.6) + (D.2.6), C1-5349: I.A +(G.5.7) + (D.2.6), C1-5350: I.A + (G.5.8) + (D.2.6), C1-5351: I.A +(G.5.9) + (D.2.6), C1-5352: I.A + (G.5.10) + (D.2.6), C1-5353: I.A +(G.5.11) + (D.2.6), C1-5354: I.A + (H.1.5) + (D.2.6), C1- 5355: I.A +(H.1.7) + (D.2.6), C1-5356: I.A + (H.2.2) + (D.2.6), C1-5357: I.A +(H.2.3) + (D.2.6), C1-5358: I.A + (H.2.5) + (D.2.6), C1-5359: I.A +(H.2.7) + (D.2.6), C1-5360: I.A + (H.2.8) + (D.2.6), C1-5361: I.A +(H.3.2) + (D.2.6), C1-5362: I.A + (H.3.4) + (D.2.6), C1-5363: I.A +(H.3.5) + (D.2.6), C1-5364: I.A + (H.4.9) + (D.2.6), C1-5365: I.A +(H.4.10) + (D.2.6), C1-5366: I.A + (I.2.2) + (D.2.6), C1-5367: I.A +(I.2.5) + (D.2.6), C1-5368: I.A + (J.1.2) + (D.2.6), C1-5369: I.A +(J.1.5) + (D.2.6), C1-5370: I.A + (J.1.8) + (D.2.6), C1-5371: I.A +(J.1.11) + (D.2.6), C1- 5372: I.A + (J.1.12) + (D.2.6), C1-5373: I.A +(K.1.3) + (D.2.6), C1-5374: I.A + 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C1-5462: I.A + (H.1.7) + (D.2.7), C1-5463: I.A +(H.2.2) + (D.2.7), C1-5464: I.A + (H.2.3) + (D.2.7), C1-5465: I.A +(H.2.5) + (D.2.7), C1-5466: I.A + (H.2.7) + (D.2.7), C1-5467: I.A +(H.2.8) + (D.2.7), C1- 5468: I.A + (H.3.2) + (D.2.7), C1-5469: I.A +(H.3.4) + (D.2.7), C1-5470: I.A + (H.3.5) + (D.2.7), C1-5471: I.A +(H.4.9) + (D.2.7), C1-5472: I.A + (H.4.10) + (D.2.7), C1-5473: I.A +(I.2.2) + (D.2.7), C1-5474: I.A + (I.2.5) + (D.2.7), C1-5475: I.A +(J.1.2) + (D.2.7), C1-5476: I.A + (J.1.5) + (D.2.7), C1-5477: I.A +(J.1.8) + (D.2.7), C1-5478: I.A + (J.1.11) + (D.2.7), C1-5479: I.A +(J.1.12) + (D.2.7), C1-5480: I.A + (K.1.3) + (D.2.7), C1-5481: I.A +(K.1.29) + (D.2.7), C1-5482: I.A + (K.1.30) + (D.2.7), C1-5483: I.A +(K.1.31) + (D.2.7), C1-5484: I.A + (K.1.32) + (D.2.7), C1- 5485: I.A +(K.1.41) + (D.2.7), C1-5486: I.A + (K.1.42) + (D.2.7), C1-5487: I.A +(K.1.44) + (D.2.7), C1-5488: I.A + (K.1.45) + (D.2.7), C1-5489: I.A +(K.1.47) + (D.2.7), C1-5490: I.A + (K.1.49) + (D.2.7), C1-5491: I.A 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(A.1.32) + (H.1.5), C1-5609: I.A +(A.1.35) + (H.1.5), C1-5610: I.A + (A.2.1) + (H.1.5), C1-5611: I.A +(A.2.3) + (H.1.5), C1-5612: I.A + (A.2.5) + (H.1.5), C1-5613: I.A +(A.3.11) + (H.1.5), C1-5614: I.A + (A.3.12) + (H.1.5), C1-5615: I.A +(A.3.15) + (H.1.5), C1- 5616: I.A + (A.3.16) + (H.1.5), C1-5617: I.A +(A.3.18) + (H.1.5), C1-5618: I.A + (A.3.19) + (H.1.5), C1-5619: I.A +(A.3.20) + (H.1.5), C1-5620: I.A + (A.3.21) + (H.1.5), C1-5621: I.A +(A.3.22) + (H.1.5), C1-5622: I.A + (A.3.23) + (H.1.5), C1-5623: I.A +(A.3.25) + (H.1.5), C1- 5624: I.A + (A.3.26) + (H.1.5), C1-5625: I.A +(A.3.27) + (H.1.5), C1-5626: I.A + (A.4.5) + (H.1.5), C1-5627: I.A +(A.4.11) + (H.1.5), C1-5628: I.A + (B.1.10) + (H.1.5), C1-5629: I.A +(B.1.11) + (H.1.5), C1-5630: I.A + (B.1.12) + (H.1.5), C1-5631: I.A +(B.1.13) + (H.1.5), C1- 5632: I.A + (B.1.18) + (H.1.5), C1-5633: I.A +(B.1.21) + (H.1.5), C1-5634: I.A + (B.1.26) + (H.1.5), C1-5635: I.A +(B.1.33) + (H.1.5), C1-5636: I.A + (B.1.34) + (H.1.5), C1-5637: I.A 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C1-5667: I.A +(G.5.6) + (H.1.5), C1- 5668: I.A + (G.5.7) + (H.1.5), C1-5669: I.A +(G.5.8) + (H.1.5), C1-5670: I.A + (G.5.9) + (H.1.5), C1-5671: I.A +(G.5.10) + (H.1.5), C1-5672: I.A + (G.5.11) + (H.1.5), C1-5673: I.A +(H.1.7) + (H.1.5), C1-5674: I.A + (H.2.2) + (H.1.5), C1-5675: I.A +(H.2.3) + (H.1.5), C1-5676: I.A + (H.2.5) + (H.1.5), C1-5677: I.A +(H.2.7) + (H.1.5), C1-5678: I.A + (H.2.8) + (H.1.5), C1-5679: I.A +(H.3.2) + (H.1.5), C1-5680: I.A + (H.3.4) + (H.1.5), C1-5681: I.A +(H.3.5) + (H.1.5), C1- 5682: I.A + (H.4.9) + (H.1.5), C1-5683: I.A +(H.4.10) + (H.1.5), C1-5684: I.A + (I.2.2) + (H.1.5), C1-5685: I.A +(I.2.5) + (H.1.5), C1-5686: I.A + (J.1.2) + (H.1.5), C1-5687: I.A +(J.1.5) + (H.1.5), C1-5688: I.A + (J.1.8) + (H.1.5), C1-5689: I.A +(J.1.11) + (H.1.5), C1-5690: I.A + (J.1.12) + (H.1.5), C1-5691: I.A +(K.1.3) + (H.1.5), C1-5692: I.A + (K.1.29) + (H.1.5), C1-5693: I.A +(K.1.30) + (H.1.5), C1-5694: I.A + (K.1.31) + (H.1.5), C1-5695: I.A +(K.1.32) + (H.1.5), C1- 5696: I.A + (K.1.41) + (H.1.5), C1-5697: I.A +(K.1.42) + (H.1.5), C1-5698: I.A + (K.1.44) + (H.1.5), C1-5699: I.A +(K.1.45) + (H.1.5), C1-5700: I.A + (K.1.47) + (H.1.5), C1-5701: I.A +(K.1.49) + (H.1.5), C1-5702: I.A + (K.1.53) + (H.1.5), C1-5703: I.A +(K.1.54) + (H.1.5), C1- 5704: I.A + (A.1.4) + (H.1.7), C1-5705: I.A +(A.1.12) + (H.1.7), C1-5706: I.A + (A.1.21) + (H.1.7), C1-5707: I.A +(A.1,21a) + (H.1.7), C1-5708: I.A + (A.1.24) + (H.1.7), C1-5709: I.A +(A.1.26) + (H.1.7), C1-5710: I.A + (A.1.27) + (H.1.7), C1-5711: I.A +(A.1.30) + (H.1.7), C1- 5712: I.A + (A.1.31) + (H.1.7), C1-5713: I.A +(A.1.32) + (H.1.7), C1-5714: I.A + (A.1.35) + (H.1.7), C1-5715: I.A +(A.2.1) + (H.1.7), C1-5716: I.A + (A.2.3) + (H.1.7), C1-5717: I.A +(A.2.5) + (H.1.7), C1-5718: I.A + (A.3.11) + (H.1.7), C1-5719: I.A +(A.3.12) + (H.1.7), C1-5720: I.A + (A.3.15) + (H.1.7), C1-5721: I.A +(A.3.16) + (H.1.7), C1-5722: I.A + (A.3.18) + (H.1.7), C1- 5723: I.A +(A.3.19) + (H.1.7), C1-5724: I.A + (A.3.20) + (H.1.7), C1-5725: I.A 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5784: I.A + (H.3.4) + (H.1.7), C1-5785: I.A +(H.3.5) + (H.1.7), C1-5786: I.A + (H.4.9) + (H.1.7), C1-5787: I.A +(H.4.10) + (H.1.7), C1-5788: I.A + (I.2.2) + (H.1.7), C1-5789: I.A +(I.2.5) + (H.1.7), C1-5790: I.A + (J.1.2) + (H.1.7), C1-5791: I.A +(J.1.5) + (H.1.7), C1-5792: I.A + (J.1.8) + (H.1.7), C1-5793: I.A +(J.1.11) + (H.1.7), C1-5794: I.A + (J.1.12) + (H.1.7), C1-5795: I.A +(K.1.3) + (H.1.7), C1-5796: I.A + (K.1.29) + (H.1.7), C1-5797: I.A +(K.1.30) + (H.1.7), C1-5798: I.A + (K.1.31) + (H.1.7), C1-5799: I.A +(K.1.32) + (H.1.7), C1-5800: I.A + (K.1.41) + (H.1.7), C1- 5801: I.A +(K.1.42) + (H.1.7), C1-5802: I.A + (K.1.44) + (H.1.7), C1-5803: I.A +(K.1.45) + (H.1.7), C1-5804: I.A + (K.1.47) + (H.1.7), C1-5805: I.A +(K.1.49) + (H.1.7), C1-5806: I.A + (K.1.53) + (H.1.7), C1-5807: I.A +(K.1.54) + (H.1.7), C1-5808: I.A + (A.1.4) + (H.2.2), C1-5809: I.A +(A.1.12) + (H.2.2), C1-5810: I.A + (A.1.21) + (H.2.2), C1-5811: I.A +(A.1.21a) + (H.2.2), C1-5812: I.A + (A.1.24) + (H.2.2), C1-5813: I.A +(A.1.26) + (H.2.2), C1-5814: I.A + (A.1.27) + (H.2.2), C1-5815: I.A +(A.1.30) + (H.2.2), C1-5816: I.A + (A.1.31) + (H.2.2), C1-5817: I.A +(A.1.32) + (H.2.2), C1-5818: I.A + (A.1.35) + (H.2.2), C1-5819: I.A +(A.2.1) + (H.2.2), C1-5820: I.A + (A.2.3) + (H.2.2), C1-5821: I.A +(A.2.5) + (H.2.2), C1-5822: I.A + (A.3.11) + (H.2.2), C1- 5823: I.A +(A.3.12) + (H.2.2), C1-5824: I.A + (A.3.15) + (H.2.2), C1-5825: I.A +(A.3.16) + (H.2.2), C1-5826: I.A + (A.3.18) + (H.2.2), C1-5827: I.A +(A.3.19) + (H.2.2), C1-5828: I.A + (A.3.20) + (H.2.2), C1-5829: I.A +(A.3.21) + (H.2.2), C1-5830: I.A + (A.3.22) + (H.2.2), C1- 5831: I.A +(A.3.23) + (H.2.2), C1-5832: I.A + (A.3.25) + (H.2.2), C1-5833: I.A +(A.3.26) + (H.2.2), C1-5834: I.A + (A.3.27) + (H.2.2), C1-5835: I.A +(A.4.5) + (H.2.2), C1-5836: I.A + (A.4.11) + (H.2.2), C1-5837: I.A +(B.1.10) + (H.2.2), C1-5838: I.A + (B.1.11) + (H.2.2), C1- 5839: I.A +(B.1.12) + (H.2.2), C1-5840: I.A + (B.1.13) + (H.2.2), C1-5841: I.A +(B.1.18) + (H.2.2), C1-5842: 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(H.2.2), C1-5872: I.A + (G.5.2) + (H.2.2), C1-5873: I.A +(G.5.3) + (H.2.2), C1-5874: I.A + (G.5.4) + (H.2.2), C1- 5875: I.A +(G.5.5) + (H.2.2), C1-5876: I.A + (G.5.6) + (H.2.2), C1-5877: I.A +(G.5.7) + (H.2.2), C1-5878: I.A + (G.5.8) + (H.2.2), C1-5879: I.A +(G.5.9) + (H.2.2), C1-5880: I.A + (G.5.10) + (H.2.2), C1-5881: I.A +(G.5.11) + (H.2.2), C1-5882: I.A + (H.2.3) + (H.2.2), C1-5883: I.A +(H.2.5) + (H.2.2), C1-5884: I.A + (H.2.7) + (H.2.2), C1-5885: I.A +(H.2.8) + (H.2.2), C1-5886: I.A + (H.3.2) + (H.2.2), C1-5887: I.A +(H.3.4) + (H.2.2), C1-5888: I.A + (H.3.5) + (H.2.2), C1- 5889: I.A +(H.4.9) + (H.2.2), C1-5890: I.A + (H.4.10) + (H.2.2), C1-5891: I.A +(I.2.2) + (H.2.2), C1-5892: I.A + (I.2.5) + (H.2.2), C1-5893: I.A +(J.1.2) + (H.2.2), C1-5894: I.A + (J.1.5) + (H.2.2), C1-5895: I.A +(J.1.8) + (H.2.2), C1-5896: I.A + (J.1.11) + (H.2.2), C1-5897: I.A +(J.1.12) + (H.2.2), C1-5898: I.A + (K.1.3) + (H.2.2), C1-5899: I.A +(K.1.29) + (H.2.2), C1-5900: I.A + (K.1.30) + (H.2.2), C1-5901: I.A +(K.1.31) + (H.2.2), C1-5902: I.A + (K.1.32) + (H.2.2), C1- 5903: I.A +(K.1.41) + (H.2.2), C1-5904: I.A + (K.1.42) + (H.2.2), C1-5905: I.A +(K.1.44) + (H.2.2), C1-5906: I.A + (K.1.45) + (H.2.2), C1-5907: I.A +(K.1.47) + (H.2.2), C1-5908: I.A + (K.1.49) + (H.2.2), C1-5909: I.A +(K.1.53) + (H.2.2), C1-5910: I.A + (K.1.54) + (H.2.2), C1- 5911: I.A +(A.1.4) + (H.3.2), C1-5912: I.A + (A.1.12) + (H.3.2), C1-5913: I.A +(A.1.21) + (H.3.2), C1-5914: I.A + (A.1,21a) + (H.3.2), C1-5915: I.A +(A.1.24) + (H.3.2), C1-5916: I.A + (A.1.26) + (H.3.2), C1-5917: I.A +(A.1.27) + (H.3.2), C1-5918: I.A + (A.1.30) + (H.3.2), C1- 5919: I.A +(A.1.31) + (H.3.2), C1-5920: I.A + (A.1.32) + (H.3.2), C1-5921: I.A +(A.1.35) + (H.3.2), C1-5922: I.A + (A.2.1) + (H.3.2), C1-5923: I.A +(A.2.3) + (H.3.2), C1-5924: I.A + (A.2.5) + (H.3.2), C1-5925: I.A +(A.3.11) + (H.3.2), C1-5926: I.A + (A.3.12) + (H.3.2), C1-5927: I.A +(A.3.15) + (H.3.2), C1-5928: I.A + (A.3.16) + (H.3.2), C1-5929: I.A +(A.3.18) + (H.3.2), C1- 5930: I.A + (A.3.19) + (H.3.2), C1-5931: I.A +(A.3.20) + (H.3.2), C1-5932: I.A + (A.3.21) + (H.3.2), C1-5933: I.A +(A.3.22) + (H.3.2), C1-5934: I.A + (A.3.23) + (H.3.2), C1-5935: I.A +(A.3.25) + (H.3.2), C1-5936: I.A + (A.3.26) + (H.3.2), C1-5937: I.A +(A.3.27) + (H.3.2), C1- 5938: I.A + (A.4.5) + (H.3.2), C1-5939: I.A +(A.4.11) + (H.3.2), C1-5940: I.A + (B.1.10) + (H.3.2), C1-5941: I.A +(B.1.11) + (H.3.2), C1-5942: I.A + (B.1.12) + (H.3.2), C1-5943: I.A +(B.1.13) + (H.3.2), C1-5944: I.A + (B.1.18) + (H.3.2), C1-5945: I.A +(B.1.21) + (H.3.2), C1- 5946: I.A + (B.1.26) + (H.3.2), C1-5947: I.A +(B.1.33) + (H.3.2), C1-5948: I.A + (B.1.34) + (H.3.2), C1-5949: I.A +(B.1.37) + (H.3.2), C1-5950: I.A + (B.1.43) + (H.3.2), C1-5951: I.A +(B.1.46) + (H.3.2), C1-5952: I.A + (B.2.5) + (H.3.2), C1-5953: I.A +(B.2.8) + (H.3.2), C1-5954: I.A + (C.1.1) + (H.3.2), C1-5955: I.A +(C.1.2) + (H.3.2), C1-5956: I.A + (C.1.4) + (H.3.2), C1- 5957: I.A +(C.1.5) + (H.3.2), C1-5958: I.A + (C.2.6) + (H.3.2), C1-5959: I.A +(C.2.7) + (H.3.2), C1-5960: I.A + (C.2.8) + (H.3.2), C1-5961: I.A +(D.1.1) + (H.3.2), C1-5962: I.A + (D.1.2) + (H.3.2), C1-5963: I.A +(D.1.5) + (H.3.2), C1-5964: I.A + (D.2.4) + (H.3.2), C1-5965: I.A +(E.1.3) + (H.3.2), C1-5966: I.A + (E.2.2) + (H.3.2), C1-5967: I.A +(E.2.3) + (H.3.2), C1-5968: I.A + (F.1.2) + (H.3.2), C1-5969: I.A +(F.1.4) + (H.3.2), C1-5970: I.A + (F.1.5) + (H.3.2), C1-5971: I.A +(G.3.1) + (H.3.2), C1-5972: I.A + (G.3.3) + (H.3.2), C1-5973: I.A +(G.3.6) + (H.3.2), C1-5974: I.A + (G.5.1) + (H.3.2), C1-5975: I.A +(G.5.2) + (H.3.2), C1-5976: I.A + (G.5.3) + (H.3.2), C1- 5977: I.A +(G.5.4) + (H.3.2), C1-5978: I.A + (G.5.5) + (H.3.2), C1-5979: I.A +(G.5.6) + (H.3.2), C1-5980: I.A + (G.5.7) + (H.3.2), C1-5981: I.A +(G.5.8) + (H.3.2), C1-5982: I.A + (G.5.9) + (H.3.2), C1-5983: I.A +(G.5.10) + (H.3.2), C1-5984: I.A + (G.5.11) + (H.3.2), C1-5985: I.A +(H.2.3) + (H.3.2), C1-5986: I.A + (H.2.5) + (H.3.2), C1-5987: I.A +(H.2.7) + (H.3.2), C1-5988: I.A + (H.2.8) + (H.3.2), C1-5989: I.A +(H.3.4) + (H.3.2), C1-5990: I.A + (H.3.5) + (H.3.2), C1- 5991: I.A +(H.4.9) + (H.3.2), C1-5992: I.A + (H.4.10) + (H.3.2), C1-5993: I.A +(I.2.2) + (H.3.2), C1-5994: I.A + (I.2.5) + (H.3.2), C1-5995: I.A +(J.1.2) + (H.3.2), C1-5996: I.A + (J.1.5) + (H.3.2), C1-5997: I.A +(J.1.8) + (H.3.2), C1-5998: I.A + (J.1.11) + (H.3.2), C1-5999: I.A +(J.1.12) + (H.3.2), C1-6000: I.A + (K.1.3) + (H.3.2), C1-6001: I.A +(K.1.29) + (H.3.2), C1-6002: I.A + (K.1.30) + (H.3.2), C1-6003: I.A +(K.1.31) + (H.3.2), C1-6004: I.A + (K.1.32) + (H.3.2), C1- 6005: I.A +(K.1.41) + (H.3.2), C1-6006: I.A + (K.1.42) + (H.3.2), C1-6007: I.A +(K.1.44) + (H.3.2), C1-6008: I.A + (K.1.45) + (H.3.2), C1-6009: I.A +(K.1.47) + (H.3.2), C1-6010: I.A + (K.1.49) + (H.3.2), C1-6011: I.A +(K.1.53) + (H.3.2), C1-6012: I.A + (K.1.54) + (H.3.2), C1- 6013: I.A +(A.1.4) + (H.3.5), C1-6014: I.A + (A.1.12) + (H.3.5), C1-6015: I.A +(A.1.21) + (H.3.5), C1-6016: I.A + (A.1,21a) + (H.3.5), C1-6017: I.A +(A.1.24) + (H.3.5), C1-6018: I.A + (A.1.26) + (H.3.5), C1-6019: I.A +(A.1.27) + (H.3.5), C1-6020: I.A + (A.1.30) + (H.3.5), C1- 6021: I.A +(A.1.31) + (H.3.5), C1-6022: I.A + (A.1.32) + (H.3.5), C1-6023: I.A +(A.1.35) + (H.3.5), C1-6024: I.A + (A.2.1) + (H.3.5), C1-6025: I.A +(A.2.3) + (H.3.5), C1-6026: I.A + (A.2.5) + (H.3.5), C1-6027: I.A +(A.3.11) + (H.3.5), C1-6028: I.A + (A.3.12) + (H.3.5), C1-6029: I.A +(A.3.15) + (H.3.5), C1-6030: I.A + (A.3.16) + (H.3.5), C1-6031: I.A +(A.3.18) + (H.3.5), C1- 6032: I.A + (A.3.19) + (H.3.5), C1-6033: I.A +(A.3.20) + (H.3.5), C1-6034: I.A + (A.3.21) + (H.3.5), C1-6035: I.A +(A.3.22) + (H.3.5), C1-6036: I.A + (A.3.23) + (H.3.5), C1-6037: I.A +(A.3.25) + (H.3.5), C1-6038: I.A + (A.3.26) + (H.3.5), C1-6039: I.A +(A.3.27) + (H.3.5), C1- 6040: I.A + (A.4.5) + (H.3.5), C1-6041: I.A +(A.4.11) + (H.3.5), C1-6042: I.A + (B.1.10) + (H.3.5), C1-6043: I.A +(B.1.11) + (H.3.5), C1-6044: I.A + (B.1.12) + (H.3.5), C1-6045: I.A +(B.1.13) + (H.3.5), C1-6046: I.A + (B.1.18) + (H.3.5), C1-6047: I.A +(B.1.21) + (H.3.5), C1- 6048: I.A + (B.1.26) + (H.3.5), C1-6049: I.A +(B.1.33) + (H.3.5), C1-6050: I.A + (B.1.34) + (H.3.5), C1-6051: I.A +(B.1.37) + (H.3.5), C1-6052: I.A + (B.1.43) + (H.3.5), C1-6053: I.A +(B.1.46) + (H.3.5), C1-6054: I.A + (B.2.5) + (H.3.5), C1-6055: I.A +(B.2.8) + (H.3.5), C1-6056: I.A + (C.1.1) + (H.3.5), C1-6057: I.A +(C.1.2) + (H.3.5), C1-6058: I.A + (C.1.4) + (H.3.5), C1- 6059: I.A +(C.1.5) + (H.3.5), C1-6060: I.A + (C.2.6) + (H.3.5), C1-6061: I.A +(C.2.7) + (H.3.5), C1-6062: I.A + (C.2.8) + (H.3.5), C1-6063: I.A +(D.1.1) + (H.3.5), C1-6064: I.A + (D.1.2) + (H.3.5), C1-6065: I.A +(D.1.5) + (H.3.5), C1-6066: I.A + (D.2.4) + (H.3.5), C1-6067: I.A +(E.1.3) + (H.3.5), C1-6068: I.A + (E.2.2) + (H.3.5), C1-6069: I.A +(E.2.3) + (H.3.5), C1-6070: I.A + (F.1.2) + (H.3.5), C1-6071: I.A +(F.1.4) + (H.3.5), C1-6072: I.A + (F.1.5) + (H.3.5), C1-6073: I.A +(G.3.1) + (H.3.5), C1-6074: I.A + (G.3.3) + (H.3.5), C1-6075: I.A +(G.3.6) + (H.3.5), C1-6076: I.A + 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C1-6620: I.A + (B.1.18) + (K.1.42),C1-6621: I.A + (B.1.21) + (K.1.42), C1-6622: I.A + (B.1.26) + (K.1.42),C1-6623: I.A + (B.1.33) + (K.1.42), C1-6624: I.A + (B.1.34) + (K.1.42),C1-6625: I.A + (B.1.37) + (K.1.42), C1-6626: I.A + (B.1.43) + (K.1.42),C1- 6627: I.A + (B.1.46) + (K.1.42), C1-6628: I.A + (B.2.5) + (K.1.42),C1-6629: I.A + (B.2.8) + (K.1.42), C1-6630: I.A + (C.1.1) + (K.1.42),C1-6631: I.A + (C.1.2) + (K.1.42), C1-6632: I.A + (C.1.4) + (K.1.42),C1-6633: I.A + (C.1.5) + (K.1.42), C1-6634: I.A + (C.2.6) + (K.1.42),C1- 6635: I.A + (C.2.7) + (K.1.42), C1-6636: I.A + (C.2.8) + (K.1.42),C1-6637: I.A + (D.1.1) + (K.1.42), C1-6638: I.A + (D.1.2) + (K.1.42),C1-6639: I.A + (D.1.5) + (K.1.42), C1-6640: I.A + (D.2.4) + (K.1.42),C1-6641: I.A + (E.1.3) + (K.1.42), C1-6642: I.A + (E.2.2) + (K.1.42),C1-6643: I.A + (E.2.3) + (K.1.42), C1-6644: I.A + (F.1.2) + (K.1.42),C1-6645: I.A + (F.1.4) + (K.1.42), C1- 6646: I.A + (F.1.5) + (K.1.42),C1-6647: I.A + (G.3.1) + (K.1.42), C1-6648: I.A + (G.3.3) + (K.1.42),C1-6649: I.A + (G.3.6) + (K.1.42), C1-6650: I.A + (G.5.1) + (K.1.42),C1-6651: I.A + (G.5.2) + (K.1.42), C1-6652: I.A + (G.5.3) + (K.1.42),C1-6653: I.A + (G.5.4) + (K.1.42), C1- 6654: I.A + (G.5.5) + (K.1.42),C1-6655: I.A + (G.5.6) + (K.1.42), C1-6656: I.A + (G.5.7) + (K.1.42),C1-6657: I.A + (G.5.8) + (K.1.42), C1-6658: I.A + (G.5.9) + (K.1.42),C1-6659: I.A + (G.5.10) + (K.1.42), C1-6660: I.A + (G.5.11) + (K.1.42),C1-6661: I.A + (H.2.3) + (K.1.42), C1- 6662: I.A + (H.2.5) + (K.1.42),C1-6663: I.A + (H.2.7) + (K.1.42), C1-6664: I.A + (H.2.8) + (K.1.42),C1-6665: I.A + (H.3.4) + (K.1.42), C1-6666: I.A + (H.4.9) + (K.1.42),C1-6667: I.A + (H.4.10) + (K.1.42), C1-6668: I.A + (I.2.2) + (K.1.42),C1-6669: I.A + (I.2.5) + (K.1.42), C1-6670: I.A + (J.1.2) + (K.1.42),C1-6671: I.A + (J.1.5) + (K.1.42), C1-6672: I.A + (J.1.8) + (K.1.42),C1- 6673: I.A + (J.1.11) + (K.1.42), C1-6674: I.A + (J.1.12) + (K.1.42),C1-6675: I.A + (K.1.41) + (K.1.42), C1-6676: I.A + (K.1.44) + (K.1.42),C1-6677: I.A + (K.1.45) + (K.1.42), C1-6678: I.A + (K.1.47) + (K.1.42),C1-6679: I.A + (K.1.49) + (K.1.42), C1-6680: I.A + (A.1.4) + (K.1.53),C1- 6681: I.A + (A.1.12) + (K.1.53), C1-6682: I.A + (A.1.21) + (K.1.53),C1-6683: I.A + (A.1,21a) + (K.1.53), C1-6684: I.A + (A.1.24) + (K.1.53),C1-6685: I.A + (A.1.26) + (K.1.53), C1-6686: I.A + (A.1.27) + (K.1.53),C1-6687: I.A + (A.1.30) + (K.1.53), C1-6688: I.A + (A.1.31) + (K.1.53),C1- 6689: I.A + (A.1.32) + (K.1.53), C1-6690: I.A + (A.1.35) + (K.1.53),C1-6691: I.A + (A.2.1) + (K.1.53), C1-6692: I.A + (A.2.3) + (K.1.53),C1-6693: I.A + (A.2.5) + (K.1.53), C1-6694: I.A + (A.3.11) + (K.1.53),C1-6695: I.A + (A.3.12) + (K.1.53), C1-6696: I.A + (A.3.15) + (K.1.53),C1- 6697: I.A + (A.3.16) + (K.1.53), C1-6698: I.A + (A.3.18) + (K.1.53),C1-6699: I.A + (A.3.19) + (K.1.53), C1-6700: I.A + (A.3.20) + (K.1.53),C1-6701: I.A + (A.3.21) + (K.1.53), C1-6702: I.A + (A.3.22) + (K.1.53),C1-6703: I.A + (A.3.23) + (K.1.53), C1-6704: I.A + (A.3.25) + (K.1.53),C1- 6705: I.A + (A.3.26) + (K.1.53), C1-6706: I.A + (A.3.27) + (K.1.53),C1-6707: I.A + (A.4.5) + (K.1.53), C1-6708: I.A + (A.4.11) + (K.1.53),C1-6709: I.A + (B.1.10) + (K.1.53), C1-6710: I.A + (B.1.11) + (K.1.53),C1-6711: I.A + (B.1.12) + (K.1.53), C1-6712: I.A + (B.1.13) + (K.1.53),C1- 6713: I.A + (B.1.18) + (K.1.53), C1-6714: I.A + (B.1.21) + (K.1.53),C1-6715: I.A + (B.1.26) + (K.1.53), C1-6716: I.A + (B.1.33) + (K.1.53),C1-6717: I.A + (B.1.34) + (K.1.53), C1-6718: I.A + (B.1.37) + (K.1.53),C1-6719: I.A + (B.1.43) + (K.1.53), C1-6720: I.A + (B.1.46) + (K.1.53),C1- 6721: I.A + (B.2.5) + (K.1.53), C1-6722: I.A + (B.2.8) + (K.1.53),C1-6723: I.A + (C.1.1) + (K.1.53), C1-6724: I.A + (C.1.2) + (K.1.53),C1-6725: I.A + (C.1.4) + (K.1.53), C1-6726: I.A + (C.1.5) + (K.1.53),C1-6727: I.A + (C.2.6) + (K.1.53), C1-6728: I.A + (C.2.7) + (K.1.53),C1- 6729: I.A + (C.2.8) + (K.1.53), C1-6730: I.A + (D.1.1) + (K.1.53),C1-6731: I.A + (D.1.2) + (K.1.53), C1-6732: I.A + (D.1.5) + (K.1.53),C1-6733: I.A + (D.2.4) + (K.1.53), C1-6734: I.A + (E.1.3) + (K.1.53),C1-6735: I.A + (E.2.2) + (K.1.53), C1-6736: I.A + (E.2.3) + (K.1.53),C1-6737: I.A + (F.1.2) + (K.1.53), C1-6738: I.A + (F.1.4) + (K.1.53),C1-6739: I.A + (F.1.5) + (K.1.53), C1- 6740: I.A + (G.3.1) + (K.1.53),C1-6741: I.A + (G.3.3) + (K.1.53), C1-6742: I.A + (G.3.6) + (K.1.53),C1-6743: I.A + (G.5.1) + (K.1.53), C1-6744: I.A + (G.5.2) + (K.1.53),C1-6745: I.A + (G.5.3) + (K.1.53), C1-6746: I.A + (G.5.4) + (K.1.53),C1-6747: I.A + (G.5.5) + (K.1.53), C1- 6748: I.A + (G.5.6) + (K.1.53),C1-6749: I.A + (G.5.7) + (K.1.53), C1-6750: I.A + (G.5.8) + (K.1.53),C1-6751: I.A + (G.5.9) + (K.1.53), C1-6752: I.A + (G.5.10) + (K.1.53),C1-6753: I.A + (G.5.11) + (K.1.53), C1-6754: I.A + (H.2.3) + (K.1.53),C1-6755: I.A + (H.2.5) + (K.1.53), C1- 6756: I.A + (H.2.7) + (K.1.53),C1-6757: I.A + (H.2.8) + (K.1.53), C1-6758: I.A + (H.3.4) + (K.1.53),C1-6759: I.A + (H.4.9) + (K.1.53), C1-6760: I.A + (H.4.10) + (K.1.53),C1-6761: I.A + (I.2.2) + (K.1.53), C1-6762: I.A + (I.2.5) + (K.1.53),C1-6763: I.A + (J.1.2) + (K.1.53), C1-6764: I.A + (J.1.5) + (K.1.53),C1-6765: I.A + (J.1.8) + (K.1.53), C1-6766: I.A + (J.1.11) + (K.1.53),C1- 6767: I.A + (J.1.12) + (K.1.53), C1-6768: I.A + (K.1.41) + (K.1.53),C1-6769: I.A + (K.1.44) + (K.1.53), C1-6770: I.A + (K.1.45) + (K.1.53),C1-6771: I.A + (K.1.47) + (K.1.53), C1-6772: I.A + (K.1.49) + (K.1.53),C1-6773: I.A + (A.1.4) + (K.1.54), C1-6774: I.A + (A.1.12) + (K.1.54),C1- 6775: I.A + (A.1.21) + (K.1.54), C1-6776: I.A + (A.1.21a) +(K.1.54), C1-6777: I.A + (A.1.24) + (K.1.54), C1-6778: I.A + (A.1.26) +(K.1.54), C1-6779: I.A + (A.1.27) + (K.1.54), C1-6780: I.A + (A.1.30) +(K.1.54), C1-6781: I.A + (A.1.31) + (K.1.54), C1-6782: I.A + (A.1.32) +(K.1.54), C1- 6783: I.A + (A.1.35) + (K.1.54), C1-6784: I.A + (A.2.1) +(K.1.54), C1-6785: I.A + (A.2.3) + (K.1.54), C1-6786: I.A + (A.2.5) +(K.1.54), C1-6787: I.A + (A.3.11) + (K.1.54), C1-6788: I.A + (A.3.12) +(K.1.54), C1-6789: I.A + (A.3.15) + (K.1.54), C1-6790: I.A + (A.3.16) +(K.1.54), C1- 6791: I.A + (A.3.18) + (K.1.54), C1-6792: I.A + (A.3.19) +(K.1.54), C1-6793: I.A + (A.3.20) + (K.1.54), C1-6794: I.A + (A.3.21) +(K.1.54), C1-6795: I.A + (A.3.22) + (K.1.54), C1-6796: I.A + (A.3.23) +(K.1.54), C1-6797: I.A + (A.3.25) + (K.1.54), C1-6798: I.A + (A.3.26) +(K.1.54), C1- 6799: I.A + (A.3.27) + (K.1.54), C1-6800: I.A + (A.4.5) +(K.1.54), C1-6801: I.A + (A.4.11) + (K.1.54), C1-6802: I.A + (B.1.10) +(K.1.54), C1-6803: I.A + (B.1.11) + (K.1.54), C1-6804: I.A + (B.1.12) +(K.1.54), C1-6805: I.A + (B.1.13) + (K.1.54), C1-6806: I.A + (B.1.18) +(K.1.54), C1- 6807: I.A + (B.1.21) + (K.1.54), C1-6808: I.A + (B.1.26) +(K.1.54), C1-6809: I.A + (B.1.33) + (K.1.54), C1-6810: I.A + (B.1.34) +(K.1.54), C1-6811: I.A + (B.1.37) + (K.1.54), C1-6812: I.A + (B.1.43) +(K.1.54), C1-6813: I.A + (B.1.46) + (K.1.54), C1-6814: I.A + (B.2.5) +(K.1.54), C1- 6815: I.A + (B.2.8) + (K.1.54), C1-6816: I.A + (C.1.1) +(K.1.54), C1-6817: I.A + (C.1.2) + (K.1.54), C1-6818: I.A + (C.1.4) +(K.1.54), C1-6819: I.A + (C.1.5) + (K.1.54), C1-6820: I.A + (C.2.6) +(K.1.54), C1-6821: I.A + (C.2.7) + (K.1.54), C1-6822: I.A + (C.2.8) +(K.1.54), C1- 6823: I.A + (D.1.1) + (K.1.54), C1-6824: I.A + (D.1.2) +(K.1.54), C1-6825: I.A + (D.1.5) + (K.1.54), C1-6826: I.A + (D.2.4) +(K.1.54), C1-6827: I.A + (E.1.3) + (K.1.54), C1-6828: I.A + (E.2.2) +(K.1.54), C1-6829: I.A + (E.2.3) + (K.1.54), C1-6830: I.A + (F.1.2) +(K.1.54), C1-6831: I.A + (F.1.4) + (K.1.54), C1-6832: I.A + (F.1.5) +(K.1.54), C1-6833: I.A + (G.3.1) + (K.1.54), C1- 6834: I.A + (G.3.3) +(K.1.54), C1-6835: I.A + (G.3.6) + (K.1.54), C1-6836: I.A + (G.5.1) +(K.1.54), C1-6837: I.A + (G.5.2) + (K.1.54), C1-6838: I.A + (G.5.3) +(K.1.54), C1-6839: I.A + (G.5.4) + (K.1.54), C1-6840: I.A + (G.5.5) +(K.1.54), C1-6841: I.A + (G.5.6) + (K.1.54), C1- 6842: I.A + (G.5.7) +(K.1.54), C1-6843: I.A + (G.5.8) + (K.1.54), C1-6844: I.A + (G.5.9) +(K.1.54), C1-6845: I.A + (G.5.10) + (K.1.54), C1-6846: I.A + (G.5.11) +(K.1.54), C1-6847: I.A + (H.2.3) + (K.1.54), C1-6848: I.A + (H.2.5) +(K.1.54), C1-6849: I.A + (H.2.7) + (K.1.54), C1- 6850: I.A + (H.2.8) +(K.1.54), C1-6851: I.A + (H.3.4) + (K.1.54), C1-6852: I.A + (H.4.9) +(K.1.54), C1-6853: I.A + (H.4.10) + (K.1.54), C1-6854: I.A + (I.2.2) +(K.1.54), C1-6855: I.A + (I.2.5) + (K.1.54), C1-6856: I.A + (J.1.2) +(K.1.54), C1-6857: I.A + (J.1.5) + (K.1.54), C1-6858: I.A + (J.1.8) +(K.1.54), C1-6859: I.A + (J.1.11) + (K.1.54), C1-6860: I.A + (J.1.12) +(K.1.54), C1-6861: I.A + (K.1.41) + (K.1.54), C1-6862: I.A + (K.1.44) +(K.1.54), C1-6863: I.A + (K.1.45) + (K.1.54), C1-6864: I.A + (K.1.47) +(K.1.54), C1-6865: I.A + (K.1.49) + (K.1.54).

Table C2: Mixtures C2-1 to C2-6865 are defined as mixtures C1-1 toC1-6865 of Table C1, wherein compound I.A in each mixture is replacedwith compound I.B.

Table C3: Mixtures C3-1 to C3-6865 are defined as mixtures C1-1 toC1-6865 of Table C1, wherein compound I.A in each mixture is replacedwith compound I.C.

Table C4: Mixtures C4-1 to C4-6865 are defined as mixtures C1-1 toC1-6865 of Table C1, wherein compound I.A in each mixture is replacedwith compound I.D.

Table C5: Mixtures C5-1 to C5-6865 are defined as mixtures C1-1 toC1-6865 of Table C1, wherein compound I.A in each mixture is replacedwith compound I.E.

Table C6: Mixtures C6-1 to C6-6865 are defined as mixtures C1-1 toC1-6865 of Table C1, wherein compound I.A in each mixture is replacedwith compound I.F.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII is, for example, 3:1, 1:1 or 1:3 in mixtures C1-1 to C1-6865, C2-1to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1to C6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII is, for example, 3:1, 1:1 or 1:3 in mixtures C1-1 to C1-6865, C2-1to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1to C6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures C1-1 to C1-6865, C2-1 toC2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 toC6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII is, for example, 3:1, 1:1 or 1:3 in mixtures C1-1 to C1-6865, C2-1to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1to C6-6865 of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 50:1 and 1:50 in mixtures C1-1 to C1-6865, C2-1 to C2-6865,C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 to C6-6865of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 20:1 and 1:20 in mixtures C1-1 to C1-6865, C2-1 to C2-6865,C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 to C6-6865of Tables C1 to C6.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 5:1 and 1:5 in mixtures C1-1 to C1-6865, C2-1 to C2-6865,C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 to C6-6865of Tables C1 to C6.

In embodiment to one embodiment the weight ratio of compound I tocompound II is between 5:1 and 1:5; and the weight ratio of compound Ito compound III is, for example, 3:1, 1:1 or 1:3 in mixtures C1-1 toC1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 3:1; andthe weight ratio of compound I to compound III is 3:1 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 3:1; andthe weight ratio of compound I to compound III is 1:1 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 3:1; andthe weight ratio of compound I to compound III is 1:3 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 1:1; andthe weight ratio of compound I to compound III is 3:1 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

According one embodiment the weight ratio of compound I to compound IIis 1:1; and the weight ratio of compound I to compound III is 1:1 inmixtures C1-1 to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 toC4-6865, C5-1 to C5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 1:1; andthe weight ratio of compound I to compound III is 1:3 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 1:3; andthe weight ratio of compound I to compound III is 3:1 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 1:3; andthe weight ratio of compound I to compound III is 1:1 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In embodiment the weight ratio of compound I to compound II is 1:3; andthe weight ratio of compound I to compound III is 1:3 in mixtures C1-1to C1-6865, C2-1 to C2-6865, C3-1 to C3-6865, C4-1 to C4-6865, C5-1 toC5-6865, and C6-1 to C6-6865 of Tables C1 to C6.

In a preferred embodiment the mixtures C1-1 to C1-6865, C2-1 to C2-6865,C3-1 to C3-6865, C4-1 to C4-6865, C5-1 to C5-6865, and C6-1 to C6-6865of Tables C1 to C6 and in particular when the weight ratios of compoundI to compound and of compound I and compound III are as disclosed forthese mixtures as herein before mentioned, are used against Phakopsorapachyrhizi and P. meibomiae on soybeans and/or against Pucciniatriticina, P. striiformis, P. hordei, P. graminis or P. recondita onwheat, barley or rye.

Other preferred ternary mixtures, preferably for use against Phakopsorapachyrhizi and P. meibomiae on soybeans and/or against Pucciniatriticina, P. striiformis, P. hordei, P. graminis or P. recondita onwheat, barley or rye, are listed in Table D below comprising ascomponent 1) one of the compounds I.A, I.B, I.C, I.D, I.E, I.F, I.G,I.H, I.J, I.K, I.L, I.M or I.N as defined above, and as component 2) oneof the compounds II as defined and numbered above, and as component 3) acompound III from groups A) to K) as defined herein. Preferably, thecompositions comprise the active substances in synergistically effectiveamounts. In the ternary mixtures D-1 to D-156 the components 1), 2) and3) are written down in this order (comp. 1)+comp. 2)+comp. 3)), so thatone mixture, for example mixture D1-1, comprises as component 1)compound I.A, as component 2) compound (A.1.1) and as component 3)compound (A.3.2).

TABLE D D-1: I.A + (B.1.38) + (B.2.4), D-2: I.A + (B.1.38) + (A.1.25),D-3: I.A + (B.1.38) + (A.1.14), D-4: I.A + (B.1.38) + (A.3.9), D-5:I.A + (B.1.38) + (B.1.23), D-6: I.A + (B.1.38) + (A.1.1), D-7: I.A +(B.1.38) + (A.1.34), D-8: I.A + (B.1.38) + (D.2.6), D-9: I.A + (A.3.9) +(A.1.14), D-10: I.A + (A.3.9) + (A.1.1), D-11: I.A + (A.3.9) + (A.1.25),D-12: I.A + (A.3.9) + (A.1.34), D-13: I.A + (A.3.9) + (D.2.6), D-14:I.A + (A.3.9) + (B.2.4), D-15: I.A + (A.3.9) + (H.2.2), D-16: I.A +(A.3.9) + (H.3.2), D-17: I.A + (A.3.9) + (H.1.5), D-18: I.A + (A.1.25) +(A.1.1), D-19: I.A + (A.1.25) + (A.1.14), D-20: I.A + (A.1.25) +(A.1.34), D-21: I.A + (A.1.25) + (D2.6), D-22: I.A + (A.3.9) + (B.1.23),D-23: I.A + (B.1.23) + (B.2.4), D-24: I.A + (B.1.23) + (H.2.2), D-25:I.A + (B.1.23) + (H.3.2), D-26: I.A + (B.1.23) + (H.1.5), D-27: I.B +(B.1.38) + (B.2.4), D-28: I.B + (B.1.38) + (A.1.25), D-29: I.B +(B.1.38) + (A.1.14), D-30: I.B + (B.1.38) + (A.3.9), D-31: I.B +(B.1.38) + (B.1.23), D-32: I.B + (B.1.38) + (A.1.1), D-33: I.B +(B.1.38) + (A.1.34), D-34: I.B + (B.1.38) + (D.2.6), D-35: I.B +(A.3.9) + (A.1.14), D-36: I.B + (A.3.9) + (A.1.1), D-37: I.B + (A.3.9) +(A.1.25), D-38: I.B + (A.3.9) + (A.1.34), D-39: I.B + (A.3.9) + (D.2.6),D-40: I.B + (A.3.9) + (B.2.4), D-41: I.B + (A.3.9) + (H.2.2), D-42:I.B + (A.3.9) + (H.3.2), D-43: I.B + (A.3.9) + (H.1.5), D-44: I.B +(A.1.25) + (A.1.1), D-45: I.B + (A.1.25) + (A.1.14), D-46: I.B +(A.1.25) + (A.1.34), D-47: I.B + (A.1.25) + (D2.6), D-48: I.B +(A.3.9) + (B.1.23), D-49: I.B + (B.1.23) + (B.2.4), D-50: I.B +(B.1.23) + (H.2.2), D-51: I.B + (B.1.23) + (H.3.2), D-52: I.B +(B.1.23) + (H.1.5), D-53: I.C + (B.1.38) + (B.2.4), D-54: I.C +(B.1.38) + (A.1.25), D-55: I.C + (B.1.38) + (A.1.14), D-56: I.C +(B.1.38) + (A.3.9), D-57: I.C + (B.1.38) + (B.1.23), D-58: I.C +(B.1.38) + (A.1.1), D-59: I.C + (B.1.38) + (A.1.34), D-60: I.C +(B.1.38) + (D.2.6), D-61: I.C + (A.3.9) + (A.1.14), D-62: I.C +(A.3.9) + (A.1.1), D-63: I.C + (A.3.9) + (A.1.25), D-64: I.C + (A.3.9) +(A.1.34), D-65: I.C + (A.3.9) + (D.2.6), D-66: I.C + (A.3.9) + (B.2.4),D-67: I.C + (A.3.9) + (H.2.2), D-68: I.C + (A.3.9) + (H.3.2), D-69:I.C + (A.3.9) + (H.1.5), D-70: I.C + (A.1.25) + (A.1.1), D-71: I.C +(A.1.25) + (A.1.14), D-72: I.C + (A.1.25) + (A.1.34), D-73: I.C +(A.1.25) + (D2.6), D-74: I.C + (A.3.9) + (B.1.23), D-75: I.C +(B.1.23) + (B.2.4), D-76: I.C + (B.1.23) + (H.2.2), D-77: I.C +(B.1.23) + (H.3.2), D-78: I.C + (B.1.23) + (H.1.5), D-79: I.D +(B.1.38) + (B.2.4), D-80: I.D + (B.1.38) + (A.1.25), D-81: I.D +(B.1.38) + (A.1.14), D-82: I.D + (B.1.38) + (A.3.9), D-83: I.D +(B.1.38) + (B.1.23), D-84: I.D + (B.1.38) + (A.1.1), D-85: I.D +(B.1.38) + (A.1.34), D-86: I.D + (B.1.38) + (D.2.6), D-87: I.D +(A.3.9) + (A.1.14), D-88: I.D + (A.3.9) + (A.1.1), D-89: I.D + (A.3.9) +(A.1.25), D-90: I.D + (A.3.9) + (A.1.34), D-91: I.D + (A.3.9) + (D.2.6),D-92: I.D + (A.3.9) + (B.2.4), D-93: I.D + (A.3.9) + (H.2.2), D-94:I.D + (A.3.9) + (H.3.2), D-95: I.D + (A.3.9) + (H.1.5), D-96: I.D +(A.1.25) + (A.1.1), D-97: I.D + (A.1.25) + (A.1.14), D-98: I.D +(A.1.25) + (A.1.34), D-99: I.D + (A.1.25) + (D2.6), D-100: I.D +(A.3.9) + (B.1.23), D-101: I.D + (B.1.23) + (B.2.4), D-102: I.D +(B.1.23) + (H.2.2), D-103: I.D + (B.1.23) + (H.3.2), D-104: I.D +(B.1.23) + (H.1.5), D-105: I.E + (B.1.38) + (B.2.4), D-106: I.E +(B.1.38) + (A.1.25), D-107: I.E + (B.1.38) + (A.1.14), D-108: I.E +(B.1.38) + (A.3.9), D-109: I.E + (B.1.38) + (B.1.23), D-110: I.E +(B.1.38) + (A.1.1), D-111: I.E + (B.1.38) + (A.1.34), D-112: I.E +(B.1.38) + (D.2.6), D-113: I.E + (A.3.9) + (A.1.14), D-114: I.E +(A.3.9) + (A.1.1), D-115: I.E + (A.3.9) + (A.1.25), D-116: I.E +(A.3.9) + (A.1.34), D-117: I.E + (A.3.9) + (D.2.6), D-118: I.E +(A.3.9) + (B.2.4), D-119: I.E + (A.3.9) + (H.2.2), D-120: I.E +(A.3.9) + (H.3.2), D-121: I.E + (A.3.9) + (H.1.5), D-122: I.E +(A.1.25) + (A.1.1), D-123: I.E + (A.1.25) + (A.1.14), D-124: I.E +(A.1.25) + (A.1.34), D-125: I.E + (A.1.25) + (D2.6), D-126: I.E +(A.3.9) + (B.1.23), D-127: I.E + (B.1.23) + (B.2.4), D-128: I.E +(B.1.23) + (H.2.2), D-129: I.E + (B.1.23) + (H.3.2), D-130: I.E +(B.1.23) + (H.1.5), D-131: I.F + (B.1.38) + (B.2.4), D-132: I.F +(B.1.38) + (A.1.25), D-133: I.F + (B.1.38) + (A.1.14), D-134: I.F +(B.1.38) + (A.3.9), D-135: I.F + (B.1.38) + (B.1.23), D-136: I.F +(B.1.38) + (A.1.1), D-137: I.F + (B.1.38) + (A.1.34), D-138: I.F +(B.1.38) + (D.2.6), D-139: I.F + (A.3.9) + (A.1.14), D-140: I.F +(A.3.9) + (A.1.1), D-141: I.F + (A.3.9) + (A.1.25), D-142: I.F +(A.3.9) + (A.1.34), D-143: I.F + (A.3.9) + (D.2.6), D-144: I.F +(A.3.9) + (B.2.4), D-145: I.F + (A.3.9) + (H.2.2), D-146: I.F +(A.3.9) + (H.3.2), D-147: I.F + (A.3.9) + (H.1.5), D-148: I.F +(A.1.25) + (A.1.1), D-149: I.F + (A.1.25) + (A.1.14), D-150: I.F +(A.1.25) + (A.1.34), D-151: I.F + (A.1.25) + (D2.6), D-152: I.F +(A.3.9) + (B.1.23), D-153: I.F + (B.1.23) + (B.2.4), D-154: I.F +(B.1.23) + (H.2.2), D-155: I.F + (B.1.23) + (H.3.2), D-156: I.F +(B.1.23) + (H.1.5).

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII is, for example, 3:1, 1:1 or 1:3 in mixtures D-1 to D-156 of TableD.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII is 3:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII is 1:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 100:1 and 1:100; and the weight ratio of compound I to compoundIII is 1:3 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII, is between 100:1 and 1:100 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 50:1 and 1:50 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 20:1 and 1:20 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII, is between 5:1 and 1:5 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII is 3:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII is 1:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 50:1 and 1:50; and the weight ratio of compound I to compoundIII is 1:3 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 50:1 and 1:50 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 20:1 and 1:20 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound III,is between 5:1 and 1:5 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII is 3:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII is 1:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 20:1 and 1:20; and the weight ratio of compound I to compoundIII is 1:3 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound IIIis 3:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound IIIis 1:1 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II isbetween 5:1 and 1:5; and the weight ratio of compound I to compound IIIis 1:3 in mixtures D-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 3:1;and the weight ratio of compound I to compound III is 3:1 in mixturesD-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 3:1;and the weight ratio of compound I to compound III is 1:1 in mixturesD-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 3:1;and the weight ratio of compound I to compound III is 1:3 in mixturesD-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 1:1;and the weight ratio of compound I to compound III is 3:1 in mixturesD-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 1:1;and the weight ratio of compound I to compound III is 1:1 in mixturesD-1 to D-156 of Table D.

In one embodiment the weight ratio of compound I to compound II is 1:1;and the weight ratio of compound I to compound III is 1:3 in mixturesD-1 to D-156 of Table D.

In a preferred embodiment the mixtures D-1 to D-156 of Table D and inparticular when the weight ratios of compound I to compound II and ofcompound I and compound III are as disclosed for these mixtures asherein before mentioned, are used against Phakopsora pachyrhizi and P.meibomiae on soybeans and/or against Puccinia triticina, P. striiformis,P. hordei P. graminis or P. recondita on wheat, barley or rye.

The binary and ternary mixtures and agrochemical compositions thereofaccording to the invention can, in the use form as fungicides, also bepresent together with further active substances, e. g. with herbicides,insecticides, growth regulators, fungicides or else with fertilizers, aspre-mix or, if appropriate, not until immediately prior to use (tankmix). Mixing the active compounds I, and III and the compositionscomprising the mixtures, respectively, in the use form as fungicideswith other fungicides results in many cases in an expansion of thefungicidal spectrum of activity being obtained or in a prevention offungicide resistance development. Furthermore, in many cases,synergistic effects are obtained.

The compounds of the formula I or compositions comprising said compoundsaccording to the invention and the mixtures comprising said compoundsand compositions, respectively, are suitable as fungicides. They aredistinguished by an outstanding effectiveness against a broad spectrumof phytopathogenic fungi, including soil-borne fungi, which deriveespecially from the following classes or are closely related to any ofthem: Ascomycota (Ascomycetes), for example, but not limited to thegenus Cocholiobolus, Colletotrichum, Fusarium, Microdochium,Penicillium, Phoma, Magnaporte, Zymoseptoria, and Pseudocercosporella;Basdiomycota (Basidiomycetes), for example, but not limited to the genusPhakospora, Puccinia, Rhizoctonia, Sphacelotheca, Tilletia, Typhula, andUstilago; Chytridiomycota (Chytridiomycetes), for example, but notlimited to the genus Chytridiales, and Synchytrium; Deuteromycetes (syn.Fungi imperfecti), for example, but not limited to the genus Ascochyta,Dlodia, Erysiphe, Fusarium, Phomopsis, and Pyrenophora;Peronosporomycetes (syn. Oomycetes), for example but not limited to thegenus Peronospora, Pythium, Phytophthora; Plasmodiophoromycetes, forexample but not limited to the genus Plasmodiophora; Zygomycetes, forexample, but not limited to the genus Rhizopus.

Some of the compounds of the formula I and the compositions according tothe invention are systemically effective and they can be used in cropprotection as foliar fungicides, fungicides for seed dressing and soilfungicides. Moreover, they are suitable for controlling harmful fungi,which inter alia occur in wood or roots of plants.

The compounds I and the compositions according to the invention areparticularly important in the control of a multitude of phytopathogenicfungi on various cultivated plants, such as cereals, e. g. wheat, rye,barley, triticale, oats or rice; beet, e. g. sugar beet or fodder beet;fruits, such as pomes, stone fruits or soft fruits, e. g. apples, pears,plums, peaches, almonds, cherries, strawberries, raspberries,blackberries or gooseberries; leguminous plants, such as lentils, peas,alfalfa or soybeans; oil plants, such as rape, mustard, olives,sunflowers, coconut, cocoa beans, castor oil plants, oil palms, groundnuts or soybeans; cucurbits, such as squashes, cucumber or melons; fiberplants, such as cotton, flax, hemp or jute; citrus fruit, such asoranges, lemons, grapefruits or mandarins; vegetables, such as spinach,lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes,cucurbits or paprika; lauraceous plants, such as avocados, cinnamon orcamphor; energy and raw material plants, such as corn, soybean, rape,sugar cane or oil palm; corn; tobacco; nuts; coffee; tea; bananas; vines(table grapes and grape juice grape vines); hop; turf; sweet leaf (alsocalled Stevia); natural rubber plants or ornamental and forestry plants,such as flowers, shrubs, broad-leaved trees or evergreens, e. g.conifers; and on the plant propagation material, such as seeds, and thecrop material of these plants. Preferably, compounds I and compositionsthereof, respectively are used for controlling a multitude of fungi onfield crops, such as potatoes sugar beets, tobacco, wheat, rye, barley,oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee orsugar cane; fruits; vines; ornamentals; or vegetables, such ascucumbers, tomatoes, beans or squashes.

The term “plant propagation material” is to be understood to denote allthe generative parts of the plant such as seeds and vegetative plantmaterial such as cuttings and tubers (e. g. potatoes), which can be usedfor the multiplication of the plant. This includes seeds, roots, fruits,tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants,including seedlings and young plants, which are to be transplanted aftergermination or after emergence from soil.

These young plants may also be protected before transplantation by atotal or partial treatment by immersion or pouring.

Preferably, treatment of plant propagation materials with compounds Iand compositions thereof, respectively, is used for controlling amultitude of fungi on cereals, such as wheat, rye, barley and oats;rice, corn, cotton and soybeans.

The term “cultivated plants” is to be understood as including plantswhich have been modified by breeding, mutagenesis or genetic engineeringincluding but not limiting to agricultural biotech products on themarket or in development (cf. http://cera-gmc.org/, see GM crop databasetherein).

The compounds I, and mixtures comprising them, and agrochemicalcompositions thereof, respectively, are particularly suitable forcontrolling the following plant diseases: Albugo spp. (white rust) onornamentals, vegetables (e. g. A. candida) and sunflowers (e. g. A.tragopogonis); Alternaria spp. (Alternaria leaf spot) on vegetables,rape (A. brassicola or brassicae), sugar beets (A. tenuis), fruits,rice, soybeans, potatoes (e. g. A. solani or A. alternata), tomatoes (e.g. A. solani or A. alternata) and wheat; Aphanomyces spp. on sugar beetsand vegetables; Ascochyta spp. on cereals and vegetables, e. g. A.tritici (anthracnose) on wheat and A. hordei on barley; Bipolaris andDrechslera spp. (teleomorph: Cochliobolus spp.), e. g. Southern leafblight (D. maydis) or Northern leaf blight (B. zeicola) on corn, e. g.spot blotch (B. sorokiniana) on cereals and e. g. B. oryzae on rice andturfs; Blumeria (formerly Erysiphe) graminis (powdery mildew) on cereals(e. g. on wheat or barley); Botrytis cinerea (teleomorph: Botryotiniafuckeliana: grey mold) on fruits and berries (e. g. strawberries),vegetables (e. g. lettuce, carrots, celery and cabbages), rape, flowers,vines, forestry plants and wheat; Bremia lactucae (downy mildew) onlettuce; Ceratocystis (syn. Ophiostoma) spp. (rot or wilt) onbroad-leaved trees and evergreens, e. g. C. ulmi (Dutch elm disease) onelms; Cercospora spp. (Cercospora leaf spots) on corn (e. g. Gray leafspot: C. zeae-maydis), rice, sugar beets (e. g. C. beticola), sugarcane, vegetables, coffee, soybeans (e. g. C. sojina or C. kikuchii) andrice; Cladosporium spp. on tomatoes (e. g. C. fulvum: leaf mold) andcereals, e. g. C. herbarum (black ear) on wheat; Claviceps purpurea(ergot) on cereals; Cochliobolus (anamorph: Helminthosporium ofBipolaris) spp. (leaf spots) on corn (C. carbonum), cereals (e. g. C.sativus, anamorph: B. sorokiniana) and rice (e. g. C. miyabeanus,anamorph: H. oryzae); Colletotrichum (teleomorph: Glomerella) spp.(anthracnose) on cotton (e. g. C. gossypii), corn (e. g. C. graminicola:Anthracnose stalk rot), soft fruits, potatoes (e. g. C. coccodes: blackdot), beans (e. g. C. lindemuthianum) and soybeans (e. g. C. truncatumor C. gloeosporioides); Corticium spp., e. g. C. sasakii (sheath blight)on rice; Corynespora cassiicola (leaf spots) on soybeans andornamentals; Cycloconium spp., e. g. C. oleaginum on olive trees;Cylindrocarpon spp. (e. g. fruit tree canker or young vine decline,teleomorph: Nectria or Neonectria spp.) on fruit trees, vines (e. g. C.lriodendri, teleomorph: Neonectria liriodendri: Black Foot Disease) andornamentals; Dematophora (teleomorph: Rosellinia) necatrix (root andstem rot) on soybeans; Diaporthe spp., e. g. D. phaseolorum (dampingoff) on soybeans; Drechslera (syn. Helminthosporium, teleomorph:Pyrenophora) spp. on corn, cereals, such as barley (e. g. D. teres, netblotch) and wheat (e. g. D. tritici-repentis: tan spot), rice and turf;Esca (dieback, apoplexy) on vines, caused by Formitiporia (syn.Phellinus) punctata, F. mediterranea, Phaeomoniella chlamydospora(earlier Phaeoacremonium chlamydosporum), Phaeoacremonium aleophilumand/or Botryosphaeria obtusa; Elsinoe spp. on pome fruits (E. pyri),soft fruits (E. veneta: anthracnose) and vines (E. ampelina:anthracnose); Entyloma oryzae (leaf smut) on rice; Epicoccum spp. (blackmold) on wheat; Erysiphe spp. (powdery mildew) on sugar beets (E.betae), vegetables (e. g. E. pisi), such as cucurbits (e. g. E.cichoracearum), cabbages, rape (e. g. E. cruciferarum); Eutypa lata(Eutypa canker or dieback, anamorph: Cytosporina lata, syn. Libertellablepharis) on fruit trees, vines and ornamental woods; Exserohilum (syn.Helminthosporium) spp. on corn (e. g. E. turcicum); Fusarium(teleomorph: Gibberella) spp. (wilt, root or stem rot) on variousplants, such as F. graminearum or F. culmorum (root rot, scab or headblight) on cereals (e. g. wheat or barley), F. oxysporum on tomatoes, F.solani(f. sp. glycines now syn. F. virguliforme) and F. tucumaniae andF. brasiliense each causing sudden death syndrome on soybeans, and F.verticillioides on corn; Gaeumannomyces graminis (take-all) on cereals(e. g. wheat or barley) and corn; Gibberella spp. on cereals (e. g. G.zeae) and rice (e. g. G. fujikuroi Bakanae disease); Glomerellacingulata on vines, pome fruits and other plants and G. gossypii oncotton; Grainstaining complex on rice; Gugnardia bidwellii (black rot)on vines; Gymnosporangium spp. on rosaceous plants and junipers, e. g.G. sabinae (rust) on pears; Helminthosporium spp. (syn. Drechslera,teleomorph: Cochliobolus) on corn, cereals and rice; Hemileia spp., e.g. H. vastatri (coffee leaf rust) on coffee; Isariopsis clavispora (syn.Cladosporium vitis) on vines; Macrophomina phaseolina (syn. phaseoli)(root and stem rot) on soybeans and cotton; Microdochium (syn. Fusarium)nivale (pink snow mold) on cereals (e. g. wheat or barley); Microsphaeradiffusa (powdery mildew) on soybeans; Monilinia spp., e. g. M. laxa, M.fructicola and M. fructigena (bloom and twig blight, brown rot) on stonefruits and other rosaceous plants; Mycosphaerella spp. on cereals,bananas, soft fruits and ground nuts, such as e. g. M. graminicola(anamorph: Septoria tritici, Septoria blotch) on wheat or M. fijiensis(black Sigatoka disease) on bananas; Peronospora spp. (downy mildew) oncabbage (e. g. P. brassicae), rape (e. g. P. parasitica), onions (e. g.P. destructor), tobacco (P. tabacina) and soybeans (e. g. P.manshurica); Phakopsora pachyrhizi and P. meibomiae (soybean rust) onsoybeans; Phialophora spp. e. g. on vines (e. g. P. tracheiphila and P.tetraspora) and soybeans (e. g. P. gregata: stem rot); Phoma lingam(root and stem rot) on rape and cabbage and P. betae (root rot, leafspot and damping-off) on sugar beets; Phomopsis spp. on sunflowers,vines (e. g. P. viticola: can and leaf spot) and soybeans (e. g. stemrot: P. phaseoli, teleomorph: Diaporthe phaseolorum); Physoderma maydis(brown spots) on corn; Phytophthora spp. (wilt, root, leaf, fruit andstem root) on various plants, such as paprika and cucurbits (e. g. P.capsici), soybeans (e. g. P. megasperma, syn. P. sojae), potatoes andtomatoes (e. g. P. infestans: late blight) and broad-leaved trees (e. g.P. ramorum: sudden oak death); Plasmodiophora brassicae (club root) oncabbage, rape, radish and other plants; Plasmopara spp., e. g. P.v//cola (grapevine downy mildew) on vines and P. halstedii onsunflowers; Podosphaera spp. (powdery mildew) on rosa-ceous plants, hop,pome and soft fruits, e. g. P. leucotricha on apples; Polymyxa spp., e.g. on cereals, such as barley and wheat (P. graminis) and sugar beets(P. betae) and thereby transmitted viral diseases; Pseudocercosporellaherpotrichoides (eyespot, teleomorph: Tapesia yallundae) on cereals, e.g. wheat or barley; Pseudoperonospora (downy mildew) on various plants,e. g. P. cubensis on cucurbits or P. humili on hop; Pseudopeziculatracheiphila (red fire disease or ‘rotbrenner’, anamorph: Phialophora)on vines; Puccinia spp. (rusts) on various plants, e. g. P. triticina(brown or leaf rust), P. striformis (stripe or yellow rust), P. hordei(dwarf rust), P. graminis (stem or black rust) or P. recondita (brown orleaf rust) on cereals, such as e. g. wheat, barley or rye, P. kuehnii(orange rust) on sugar cane and P. asparagion asparagus; Pyrenophora(anamorph: Drechslera) tritici-repentis (tan spot) on wheat or P. teres(net blotch) on barley; Pyricularia spp., e. g. P. oryzae (teleomorph:Magnaporthe gr/sea, rice blast) on rice and P. grisea on turf andcereals; Pythium spp. (damping-off) on turf, rice, corn, wheat, cotton,rape, sunflowers, soybeans, sugar beets, vegetables and various otherplants (e. g. P. ultimum or P. aphanidermatum); Ramularia spp., e. g. R.collo-cygni(Ramularia leaf spots, Physiological leaf spots) on barleyand R. beticola on sugar beets; Rhizoctonia spp. on cotton, rice,potatoes, turf, corn, rape, potatoes, sugar beets, vegetables andvarious other plants, e. g. R. solani (root and stem rot) on soybeans,R. solani (sheath blight) on rice or R. cerealis (Rhizoctonia springblight) on wheat or barley; Rhizopus stolonifer (black mold, soft rot)on strawberries, carrots, cabbage, vines and tomatoes; Rhynchosporiumsecalis (scald) on barley, rye and triticale; Sarocladium oryzae and S.attenuatum (sheath rot) on rice; Sclerotinia spp. (stem rot or whitemold) on vegetables and field crops, such as rape, sunflowers (e. g. S.sclerotiorum) and soybeans (e. g. S. rolfsii or S. sclerotiorum);Septoria spp. on various plants, e. g. S. glycines (brown spot) onsoybeans, S. tritici (Septoria blotch) on wheat and S. (syn.Stagonospora) nodorum (Stagonospora blotch) on cereals; Uncinula (syn.Erysiphe) necator (powdery mildew, anamorph: Oidium tuckeri) on vines;Setospaeria spp. (leaf blight) on corn (e. g. S. turcicum, syn.Helminthosporium turcicum) and turf; Sphacelotheca spp. (smut) on corn,(e. g. S. reiliana: head smut), sorghum und sugar cane; Sphaerothecafuliginea (powdery mildew) on cucurbits; Spongospora subterranea(powdery scab) on potatoes and thereby transmitted viral diseases;Stagonospora spp. on cereals, e. g. S. nodorum (Stagonospora blotch,teleomorph: Leptosphaeria [syn. Phaeosphaeria] nodorum) on wheat;Synchytrium endobioticum on potatoes (potato wart disease); Taphrinaspp., e. g. T. deformans (leaf curl disease) on peaches and T. pruni(plum pocket) on plums; Thielaviopsis spp. (black root rot) on tobacco,pome fruits, vegetables, soybeans and cotton, e. g. T. basicola (syn.Chalara elegans); Tilletia spp. (common bunt or stinking smut) oncereals, such as e. g. T. tritici (syn. T. caries, wheat bunt) and T.controversa (dwarf bunt) on wheat; Typhula incarnata (grey snow mold) onbarley or wheat; Urocystis spp., e. g. U. occulta (stem smut) on rye;Uromyces spp. (rust) on vegetables, such as beans (e. g. U.appendiculatus, syn. U. phaseoli) and sugar beets (e. g. U. betae);Ustilago spp. (loose smut) on cereals (e. g. U. nuda and U. avaenae),corn (e. g. U. maydis: corn smut) and sugar cane; Venturia spp. (scab)on apples (e. g. V. inaequalis) and pears; and Verticilium spp. (wilt)on various plants, such as fruits and ornamentals, vines, soft fruits,vegetables and field crops, e. g. V. dahilae on strawberries, rape,potatoes and tomatoes. In a preferred embodiment the compounds I, theirmixtures with other active compounds as defined herein and compositionsthereof, respectively, are particularly suitable for controlling thefollowing plant diseases: Puccinia spp. (rusts) on various plants, forexample, but not limited to P. triticina (brown or leaf rust), P.striformis (stripe or yellow rust), P. hordei (dwarf rust), P. graminis(stem or black rust) or P. recondita (brown or leaf rust) on cereals,such as e. g. wheat, barley or rye and Phakopsoraceae spp. on variousplants, in particular Phakopsorapachyrhizi and P. meibomiae (soybeanrust) on soybeans.

The compounds I and compositions thereof, respectively, are alsosuitable for controlling harmful fungi in the protection of storedproducts or harvest and in the protection of materials. The term“protection of materials” is to be understood to denote the protectionof technical and non-living materials, such as adhesives, glues, wood,paper and paperboard, textiles, leather, paint dispersions, plastics,cooling lubricants, fiber or fabrics, against the infestation anddestruction by harmful microorganisms, such as fungi and bacteria. As tothe protection of wood and other materials, the particular attention ispaid to the following harmful fungi: Ascomycetes such as Ophiostomaspp., Ceratocystis spp., Aureobasidium pullulans, Sclerophoma spp.,Chaetomium spp., Humicola spp., Petriella spp., Trichurus spp.;Basidiomycetes such as Coniophora spp., Coriolus spp., Gloeophyllumspp., Lentinus spp., Pleurotus spp., Poria spp., Serpula spp. andTyromyces spp., Deuteromycetes such as Aspergillus spp., Cladosporiumspp., Penicllium spp., Trichoderma spp., Alternaria spp., Paeciomycesspp. and Zygomycetes such as Mucor spp., and in addition in theprotection of stored products and harvest the following yeast fungi areworthy of note: Candida spp. and Saccharomyces cerevisae.

The method of treatment according to the invention can also be used inthe field of protecting stored products or harvest against attack offungi and microorganisms. According to the present invention, the term“stored products” is understood to denote natural substances of plant oranimal origin and their processed forms, which have been taken from thenatural life cycle and for which long-term protection is desired. Storedproducts of crop plant origin, such as plants or parts thereof, forexample stalks, leafs, tubers, seeds, fruits or grains, can be protectedin the freshly harvested state or in processed form, such as pre-dried,moistened, comminuted, ground, pressed or roasted, which process is alsoknown as post-harvest treatment. Also falling under the definition ofstored products is timber, whether in the form of crude timber, such asconstruction timber, electricity pylons and barriers, or in the form offinished articles, such as furniture or objects made from wood. Storedproducts of animal origin are hides, leather, furs, hairs and the like.The combinations according the present invention can preventdisadvantageous effects such as decay, discoloration or mold. Preferably“stored products” is understood to denote natural substances of plantorigin and their processed forms, more preferably fruits and theirprocessed forms, such as pomes, stone fruits, soft fruits and citrusfruits and their processed forms.

The compounds I and compositions thereof, respectively, may be used forimproving the health of a plant. The invention also relates to a methodfor improving plant health by treating a plant, its propagation materialand/or the locus where the plant is growing or is to grow with aneffective amount of compounds I and compositions thereof, respectively.

The term “plant health” is to be understood to denote a condition of theplant and/or its products which is determined by several indicatorsalone or in combination with each other such as yield (e. g. increasedbiomass and/or increased content of valuable ingredients), plant vigor(e. g. improved plant growth and/or greener leaves (“greening effect”)),quality (e. g. improved content or composition of certain ingredients)and tolerance to abiotic and/or biotic stress. The above identifiedindicators for the health condition of a plant may be interdependent ormay result from each other.

The compounds of formula I can be present in different crystalmodifications whose biological activity may differ. They are likewisesubject matter of the present invention.

The compounds I are employed as such or in form of compositions bytreating the fungi or the plants, plant propagation materials, such asseeds, soil, surfaces, materials or rooms to be protected from fungalattack with a fungicidally effective amount of the active substances.The application can be carried out both before and after the infectionof the plants, plant propagation materials, such as seeds, soil,surfaces, materials or rooms by the fungi.

Plant propagation materials may be treated with compounds I as such or acomposition comprising at least one compound I prophylactically eitherat or before planting or transplanting. The invention also relates toagrochemical compositions comprising an auxiliary and at least onecompound I according to the invention.

An agrochemical composition comprises a fungicidally effective amount ofa compound I. The term “effective amount” denotes an amount of thecomposition or of the compounds I, which is sufficient for controllingharmful fungi on cultivated plants or in the protection of materials andwhich does not result in a substantial damage to the treated plants.Such an amount can vary in a broad range and is dependent on variousfactors, such as the fungal species to be controlled, the treatedcultivated plant or material, the climatic conditions and the specificcompound I used.

The compounds I, their N-oxides and salts can be converted intocustomary types of agrochemical compositions, e. g. solutions,emulsions, suspensions, dusts, powders, pastes, granules, pressings,capsules, and mixtures thereof. Examples for composition types aresuspensions (e. g. SC, OD, FS), emulsifiable concentrates (e. g. EC),emulsions (e. g. EW, EO, ES, ME), capsules (e. g. CS, ZC), pastes,pastilles, wettable powders or dusts (e. g. WP, SP, WS, DP, DS),pressings (e. g. BR, TB, DT), granules (e. g. WG, SG, GR, FG, GG, MG),insecticidal articles (e. g. LN), as well as gel formulations for thetreatment of plant propagation materials such as seeds (e. g. GF). Theseand further compositions types are defined in the “Catalogue ofpesticide formulation types and international coding system”, TechnicalMonograph No. 2, 6^(th) Ed. May 2008, CropLife International.

The compositions are prepared in a known manner, such as described byMollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001;or Knowles, New developments in crop protection product formulation,Agrow Reports DS243, T&F Informa, London, 2005.

The binary or ternary mixtures of active compounds described herein canbe prepared as compositions comprising besides the active ingredients atleast one inert ingredient (auxiliary) by usual means, e. g. by themeans given herein for the compositions of compounds I.

Concerning usual ingredients of such compositions reference is made tothe explanations given for the compositions containing compounds I.

Suitable auxiliaries are solvents, liquid carriers, solid carriers orfillers, surfactants, dispersants, emulsifiers, wetters, adjuvants,solubilizers, penetration enhancers, protective colloids, adhesionagents, thickeners, humectants, repellents, attractants, feedingstimulants, compatibilizers, bactericides, anti-freezing agents,anti-foaming agents, colorants, tackifiers and binders.

Suitable solvents and liquid carriers are water and organic solvents,such as mineral oil fractions of medium to high boiling point, e. g.kerosene, diesel oil; oils of vegetable or animal origin; aliphatic,cyclic and aromatic hydrocarbons, e. g. toluene, paraffin,tetrahydronaphthalene, alkylated naphthalenes; alcohols, e. g. ethanol,propanol, butanol, benzyl alcohol, cyclohexanol; glycols; DMSO; ketones,e. g. cyclohexanone; esters, e. g. lactates, carbonates, fatty acidesters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides,e. g. N-methyl pyrrolidone, fatty acid dimethyl amides; and mixturesthereof.

Suitable solid carriers or fillers are mineral earths, e. g. silicates,silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite,diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate,magnesium oxide; polysaccharides, e. g. cellulose, starch; fertilizers,e. g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas;products of vegetable origin, e. g. cereal meal, tree bark meal, woodmeal, nutshell meal, and mixtures thereof.

Suitable surfactants are surface-active compounds, such as anionic,cationic, nonionic and amphoteric surfactants, block polymers,polyelectrolytes, and mixtures thereof. Such surfactants can be used asemulsifier, dispersant, solubilizer, wetter, penetration enhancer,protective colloid, or adjuvant. Examples of surfactants are listed inMcCutcheon's, Vol. 1: Emulsifiers & Detergents, McCutcheon'sDirectories, Glen Rock, USA, 2008 (International Ed. or North AmericanEd.).

Suitable anionic surfactants are alkali, alkaline earth or ammoniumsalts of sulfonates, sulfates, phosphates, carboxylates, and mixturesthereof. Examples of sulfonates are alkylaryl sulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignin sulfonates, sulfonates offatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonatesof alkoxylated arylphenols, sulfonates of condensed naphthalenes,sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenesand alkyl naphthalenes, sulfosuccinates or sulfosuccinamates. Examplesof sulfates are sulfates of fatty acids and oils, of ethoxylatedalkylphenols, of alcohols, of ethoxylated alcohols, or of fatty acidesters. Examples of phosphates are phosphate esters. Examples ofcarboxylates are alkyl carboxylates, and carboxylated alcohol oralkylphenol ethoxylates.

Suitable nonionic surfactants are alkoxylates, N-substituted fatty acidamides, amine oxides, esters, sugar-based surfactants, polymericsurfactants, and mixtures thereof. Examples of alkoxylates are compoundssuch as alcohols, alkylphenols, amines, amides, arylphenols, fatty acidsor fatty acid esters which have been alkoxylated with 1 to 50equivalents. Ethylene oxide and/or propylene oxide may be employed forthe alkoxylation, preferably ethylene oxide.

Examples of N-substituted fatty acid amides are fatty acid glucamides orfatty acid alkanolamides. Examples of esters are fatty acid esters,glycerol esters or monoglycerides.

Examples of sugar-based surfactants are sorbitans, ethoxylatedsorbitans, sucrose and glucose esters or alkylpolyglucosides. Examplesof polymeric surfactants are home- or copolymers of vinyl pyrrolidone,vinyl alcohols, or vinyl acetate.

Suitable cationic surfactants are quaternary surfactants, for examplequaternary ammonium compounds with one or two hydrophobic groups, orsalts of long-chain primary amines. Suitable amphoteric surfactants arealkylbetains and imidazolines. Suitable block polymers are blockpolymers of the A-B or A-B-A type comprising blocks of polyethyleneoxide and polypropylene oxide, or of the A-B—C type comprising alkanol,polyethylene oxide and polypropylene oxide. Suitable polyelectrolytesare polyacids or polybases. Examples of polyacids are alkali salts ofpolyacrylic acid or polyacid comb polymers. Examples of polybases arepolyvinyl amines or polyethylene amines.

Suitable adjuvants are compounds, which have a negligible or even nopesticidal activity themselves, and which improve the biologicalperformance of the compound I on the target. Examples are surfactants,mineral or vegetable oils, and other auxiliaries. Further examples arelisted by Knowles, Adjuvants and additives, Agrow Reports DS256, T&FInforma UK, 2006, chapter 5.

Suitable thickeners are polysaccharides (e. g. xanthan gum,carboxymethyl cellulose), inorganic clays (organically modified orunmodified), polycarboxylates, and silicates.

Suitable bactericides are bronopol and isothiazolinone derivatives suchas alkylisothiazolinones and benzisothiazolinones.

Suitable anti-freezing agents are ethylene glycol, propylene glycol,urea and glycerin.

Suitable anti-foaming agents are silicones, long chain alcohols, andsalts of fatty acids.

Suitable colorants (e. g. in red, blue, or green) are pigments of lowwater solubility and water-soluble dyes. Examples are inorganiccolorants (e. g. iron oxide, titan oxide, iron hexacyanoferrate) andorganic colorants (e. g. alizarin-, azo- and phthalocyanine colorants).

Suitable tackifiers or binders are polyvinyl pyrrolidones, polyvinylacetates, polyvinyl alcohols, polyacrylates, biological or syntheticwaxes, and cellulose ethers.

Examples for composition types and their preparation are:

i) Water-Soluble Concentrates (SL, LS)

10-60 wt % of a compound I and 5-15 wt % wetting agent (e. g. alcoholalkoxylates) are dissolved in water and/or in a water-soluble solvent(e. g. alcohols) ad 100 wt %. The active compound dissolves upondilution with water.

ii) Dispersible Concentrates (DC)

5-25 wt % of a compound I and 1-10 wt % dispersant (e. g. polyvinylpyrrolidone) are dissolved in organic solvent (e. g. cyclohexanone) ad100 wt %. Dilution with water gives a dispersion.

iii) Emulsifiable Concentrates (EC)

15-70 wt % of a compound I and 5-10 wt % emulsifiers (e. g. calciumdodecylbenzenesulfonate and castor oil ethoxylate) are dissolved inwater-insoluble organic solvent (e. g. aromatic hydrocarbon) ad 100 wt%. Dilution with water gives an emulsion.

iv) Emulsions (EW, EO, ES)

5-40 wt % of a compound I and 1-10 wt % emulsifiers (e. g. calciumdodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in20-40 wt % water-insoluble organic solvent (e. g. aromatic hydrocarbon).This mixture is introduced into water ad 100 wt % by means of anemulsifying machine and made into a homogeneous emulsion. Dilution withwater gives an emulsion.

v) Suspensions (SC, OD, FS)

In an agitated ball mill, 20-60 wt % of a compound I are comminuted withaddition of 2-10 wt % dispersants and wetting agents (e. g. sodiumlignosulfonate and alcohol ethoxylate), 0.1-2 wt % thickener (e. g.xanthan gum) and water ad 100 wt % to give a fine active compoundsuspension. Dilution with water gives a stable suspension of the activesubstance. For FS type composition up to 40 wt % binder (e. g. polyvinylalcohol) is added.

vi) Water-Dispersible Granules and Water-Soluble Granules (WG, SG)

50-80 wt % of a compound I are ground finely with addition ofdispersants and wetting agents (e. g. sodium lignosulfonate and alcoholethoxylate) ad 100 wt % and prepared as water-dispersible orwater-soluble granules by means of technical appliances (e. g.extrusion, spray tower, fluidized bed). Dilution with water gives astable dispersion or solution of the active substance.

vii) Water-Dispersible Powders and Water-Soluble Powders (WP, SP, WS)

50-80 wt % of a compound I are ground in a rotor-stator mill withaddition of 1-5 wt % dispersants (e. g. sodium lignosulfonate), 1-3 wt %wetting agents (e. g. alcohol ethoxylate) and solid carrier (e. g.silica gel) ad 100 wt %. Dilution with water gives a stable dispersionor solution of the active substance.

viii) Gel (GW, GF)

In an agitated ball mill, 5-25 wt % of a compound I are comminuted withaddition of 3-10 wt % dispersants (e. g. sodium lignosulfonate), 1-5 wt% thickener (e. g. carboxymethyl cellulose) and water ad 100 wt % togive a fine suspension of the active substance. Dilution with watergives a stable suspension of the active substance.

ix) Microemulsion (ME)

5-20 wt % of a compound I are added to 5-30 wt % organic solvent blend(e. g. fatty acid dimethyl amide and cyclohexanone), 10-25 wt %surfactant blend (e. g. alcohol ethoxylate and arylphenol ethoxylate),and water ad 100%. This mixture is stirred for 1 h to producespontaneously a thermodynamically stable microemulsion.

x) Microcapsules (CS)

An oil phase comprising 5-50 wt % of a compound I, 0-40 wt % waterinsoluble organic solvent (e. g. aromatic hydrocarbon), 2-15 wt %acrylic monomers (e. g. methylmethacrylate, methacrylic acid and a di-or triacrylate) are dispersed into an aqueous solution of a protectivecolloid (e. g. polyvinyl alcohol). Radical polymerization results in theformation of poly(meth)acrylate microcapsules. Alternatively, an oilphase comprising 5-50 wt % of a compound I according to the invention,0-40 wt % water insoluble organic solvent (e. g. aromatic hydrocarbon),and an isocyanate monomer (e. g. diphenylmethene-4,4′-diisocyanatae) aredispersed into an aqueous solution of a protective colloid (e. g.polyvinyl alcohol). The addition of a polyamine (e. g.hexamethylenediamine) results in the formation of polyureamicrocapsules. The monomers amount to 1-10 wt %. The wt % relate to thetotal CS composition.

xi) Dustable Powders (DP, DS)

1-10 wt % of a compound I are ground finely and mixed intimately withsolid carrier (e. g. finely divided kaolin) ad 100 wt %.

xii) Granules (GR, FG)

0.5-30 wt % of a compound I is ground finely and associated with solidcarrier (e. g. silicate) ad 100 wt %. Granulation is achieved byextrusion, spray-drying or fluidized bed.

xiii) Ultra-Low Volume Liquids (UL)

1-50 wt % of a compound I are dissolved in organic solvent (e. g.aromatic hydrocarbon) ad 100 wt %.

The compositions types i) to xiii) may optionally comprise furtherauxiliaries, such as 0.1-1 wt % bactericides, 5-15 wt % anti-freezingagents, 0.1-1 wt % anti-foaming agents, and 0.1-1 wt % colorants.

The agrochemical compositions generally comprise between 0.01 and 95%,preferably between 0.1 and 90%, more preferably between 1 and 70%, andin particular between 10 and 60%, by weight of active substance. Theactive substances are employed in a purity of from 90% to 100%,preferably from 95% to 100% (according to NMR spectrum).

For the purposes of treatment of plant propagation materials,particularly seeds, solutions for seed treatment (LS), Suspoemulsions(SE), flowable concentrates (FS), powders for dry treatment (DS),water-dispersible powders for slurry treatment (WS), water-solublepowders (SS), emulsions (ES), emulsifiable concentrates (EC), and gels(GF) are usually employed. The compositions in question give, aftertwo-to-tenfold dilution, active compound concentrations of from 0.01 to60% by weight, preferably from 0.1 to 40%, in the ready-to-usepreparations.

Application can be carried out before or during sowing. Methods forapplying compound I and compositions thereof, respectively, onto plantpropagation material, especially seeds, include dressing, coating,pelleting, dusting, and soaking as well as in-furrow applicationmethods. Preferably, compound I or the compositions thereof,respectively, are applied on to the plant propagation material by amethod such that germination is not induced, e. g. by seed dressing,pelleting, coating and dusting.

When employed in plant protection, the amounts of active substancesapplied are, depending on the kind of effect desired, from 0.001 to 2 kgper ha, preferably from 0.005 to 2 kg per ha, more preferably from 0.05to 0.9 kg per ha, and in particular from 0.1 to 0.75 kg per ha.

In treatment of plant propagation materials such as seeds, e. g. bydusting, coating or drenching seed, amounts of active compound of from0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to100 g and most preferably from 5 to 100 g, per 100 kilogram of plantpropagation material (preferably seeds) are generally required.

When used in the protection of materials or stored products, the amountof active compound applied depends on the kind of application area andon the desired effect. Amounts customarily applied in the protection ofmaterials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of activecompound per cubic meter of treated material.

Various types of oils, wetters, adjuvants, fertilizer, ormicronutrients, and further pesticides (e. g. herbicides, insecticides,fungicides, growth regulators, safeners, biopesticides) may be added tothe active substances or the compositions comprising them as premix or,if appropriate not until immediately prior to use (tank mix). Theseagents can be admixed with the compositions according to the inventionin a weight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.

A pesticide is generally a chemical or biological agent (such aspestidal active ingredient, compound, composition, virus, bacterium,antimicrobial or disinfectant) that through its effect deters,incapacitates, kills or otherwise discourages pests. Target pests caninclude insects, plant pathogens, weeds, mollusks, birds, mammals, fish,nematodes (roundworms), and microbes that destroy property, causenuisance, spread disease or are vectors for disease. The term“pesticide” includes also plant growth regulators that alter theexpected growth, flowering, or reproduction rate of plants; defoliantsthat cause leaves or other foliage to drop from a plant, usually tofacilitate harvest; desiccants that promote drying of living tissues,such as unwanted plant tops; plant activators that activate plantphysiology for defense of against certain pests; safeners that reduceunwanted herbicidal action of pesticides on crop plants; and plantgrowth promoters that affect plant physiology e.g. to increase plantgrowth, biomass, yield or any other quality parameter of the harvestablegoods of a crop plant.

The user applies the composition according to the invention usually froma predosage device, a knapsack sprayer, a spray tank, a spray plane, oran irrigation system. Usually, the agrochemical composition is made upwith water, buffer, and/or further auxiliaries to the desiredapplication concentration and the ready-to-use spray liquor or theagrochemical composition according to the invention is thus obtained.Usually, 20 to 2000 liters, preferably 50 to 400 liters, of theready-to-use spray liquor are applied per hectare of agricultural usefularea.

According to one embodiment, individual components of the compositionaccording to the invention such as parts of a kit or parts of a binaryor ternary mixture may be mixed by the user himself in a spray tank orany other kind of vessel used for applications (e. g. seed treaterdrums, seed pelleting machinery, knapsack sprayer) and furtherauxiliaries may be added, if appropriate.

Consequently, one embodiment of the invention is a kit for preparing ausable pesticidal composition, the kit comprising a) a compositioncomprising component 1) as defined herein and at least one auxiliary;and b) a composition comprising component 2) as defined herein and atleast one auxiliary; and optionally c) a composition comprising at leastone auxiliary and optionally a further active component 3) as definedherein.

Mixing the compounds I or the compositions comprising them in the useform as fungicides with other fungicides results in many cases in anexpansion of the fungicidal spectrum of activity being obtained or in aprevention of fungicide resistance development. Furthermore, in manycases, synergistic effects are obtained.

The present invention furthermore relates to agrochemical compositionscomprising a mixture of at least one compound I (component 1) and atleast one further active compound useful for plant protection, e. g.selected from the groups A) to O) (component 2), in particular onefurther fungicide, e. g. one or more fungicide from the groups A) to K),as described above, and if desired one suitable solvent or solidcarrier. Those mixtures are of particular interest, since many of themat the same application rate show higher efficiencies against harmfulfungi. Furthermore, combating harmful fungi with a mixture of compoundsI and at least one fungicide from groups A) to K), as described above,is more efficient than combating those fungi with individual compounds Ior individual fungicides from groups A) to K).

By applying compounds I together with at least one active compound fromgroups A) to O) a synergistic effect can be obtained, i.e. more thansimple addition of the individual effects is obtained (synergisticmixtures).

This can be obtained by applying the compounds I and at least onefurther active compound simultaneously, either jointly (e. g. astank-mix) or separately, or in succession, wherein the time intervalbetween the individual applications is selected to ensure that theactive compound applied first still occurs at the site of action in asufficient amount at the time of application of the further activesubstance(s). The order of application is not essential for working ofthe present invention.

When applying compound I and a pesticide II sequentially the timebetween both applications may vary e. g. between 2 hours to 7 days. Alsoa broader range is possible ranging from 0.25 hour to 30 days,preferably from 0.5 hour to 14 days, particularly from 1 hour to 7 daysor from 1.5 hours to 5 days, even more preferred from 2 hours to 1 day.

In the binary mixtures and compositions according to the invention theweight ratio of the component 1) and the component 2) generally dependsfrom the properties of the active components used, usually it is in therange of from 1:10000 to 10000:1, often it is in the range of from 1:100to 100:1, regularly in the range of from 1:50 to 50:1, preferably in therange of from 1:20 to 20:1, more preferably in the range of from 1:5 to5:1 and in particular in the range of from 1:2 to 2:1.

According to a further embodiment of the binary mixtures andcompositions, the weight ratio of the component 1) and the component 2)usually is in the range of from 1000:1 to 1:1, often in the range offrom 100:1 to 1:1, regularly in the range of from 50:1 to 1:1,preferably in the range of from 20:1 to 1:1, more preferably in therange of from 5:1 to 1:1 and in particular in the range of from 2:1 to1:1.

According to a further embodiments of the binary mixtures andcompositions, the weight ratio of the component 1) and the component 2)usually is in the range of from 1:1 to 1:1000, often in the range offrom 1:1 to 1:100, regularly in the range of from 1:1 to 1:50,preferably in the range of from 1:1 to 1:20, more preferably in therange of from 1:1 to 1:5 and in particular in the range of from 1:1 to1:2.

In the ternary mixtures, i.e. compositions according to the inventioncomprising the component 1) and component 2) and a compound III(component 3), the weight ratio of component 1) and component 2) is inthe range of from 1:100 to 100:1, regularly in the range of from 1:50 to50:1, preferably in the range of from 1:20 to 20:1, more preferably inthe range of from 1:5 to 5:1 and in particular in the range of from 1:2to 2:1, and the weight ratio of component 1) and component 3) is in therange of from 1:100 to 100:1, regularly in the range of from 1:50 to50:1, preferably in the range of from 1:20 to 20:1, more preferably inthe range of from 1:5 to 5:1 and in particular in the range of from 1:2to 2:1.

Any further active components are, if desired, added in a ratio of from20:1 to 1:20 to the component 1).

These ratios are also suitable for inventive mixtures applied by seedtreatment.

Biological Activity

The fungicidal action of the mixtures according to the invention can beshown by the tests described below. The efficacy (E) is calculated asfollows using Abbot's formula:

E=(1−α/β)·100

-   α corresponds to the fungicidal infection of the treated plants in %    and-   β corresponds to the fungicidal infection of the untreated (control)    plants in %

An efficacy of 0 means that the infection level of the treated plantscorresponds to that of the untreated control plants; an efficacy of 100means that the treated plants were not infected. The expected efficaciesof active compound combinations may be determined using Colby's formula(Colby, S.R. “Calculating synergistic and antagonistic responses ofherbicide combinations”, Weeds, 15, pp. 20-22, 1967) and compared withthe observed efficacies. Colby's formula:

E=x+y−x·y/100

-   E expected efficacy, expressed in % of the untreated control, when    using the mixture of the active compounds A and B at the    concentrations a and b-   x efficacy, expressed in % of the untreated control, when using the    active compound A at the concentration a-   y efficacy, expressed in % of the untreated control, when using the    active compound B at the concentration b.

The expression “I.B/I.C” relates to a mixture of stereoisomers 1.B andI.C.

The expression “I.H/I.J” relates to a mixture of stereoisomers I.H andI.J.

I) Fungicidal Activity Against Botrytis cinerea

The active compounds were formulated separately as a stock solutionhaving a concentration of 10000 ppm in dimethyl sulfoxide. The stocksolutions were mixed according to the ratio, pipetted onto a micro titerplate (MTP) and diluted with water to the stated concentrations. A sporesuspension of Botrytis cinerea in an aqueous biomalt oryeast-bactopeptone-sodiumacetate solution was then added. The plateswere placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7days after the inoculation. The measured parameters were compared to thegrowth of the active compound-free control variant (100%) and thefungus-free and active compound-free blank value to determine therelative growth in % of the pathogens in the respective activecompounds. These percentages were converted into efficacies.

TABLE I.1 Use examples of fungicidal activity against Botrytis cinereaof I.H/I.J as component A and components B Active mixture Code ofConcentration Efficacy (component A + B) component B A + B (ppm) (ppm)I.H/I.J + component B A.3.29 16 + 1 86 I.H/I.J + component B K.1.29 16 + 16 99 I.H/I.J + component B A.2.5 16 + 1 81 I.H/I.J + component BA.3.32 16 + 1 81 I.H/I.J + component B K.1.30 16 + 4 99 I.H/I.J +component B K.1.32 16 + 1 89 I.H/I.J + component B K.1.31 16 + 4 99I.H/I.J + Benomyl D.1.1 16 + 4 100 I.H/I.J + Bixafen A.3.3   16 + 0.2559 I.H/I.J + Boscalid A.3.4 16 + 4 85 I.H/I.J + Captan H.3.4 16 + 4 100I.H/I.J + Carbendazim D.1.2   16 + 0.25 100 I.H/I.J + Cyproconazol B.1.4 16 + 16 100 I.H/I.J + Cyprodinil E.1.1 16 + 4 72 I.H/I.J + DithianonH.4.9 16 + 1 100 I.H/I.J + Epoxiconazol B.1.8.   16 + 0.25 72 I.H/I.J +Fenpropimorph B.2.4 16 + 1 91 I.H/I.J + Fludioxonil F.1.5   16 + 0.25 98I.H/I.J + Fluindapyr A.3.28 16 + 1 78 I.H/I.J + Fluquinconazol B.1.1016 + 1 100 I.H/I.J + Penthiopyrad A.3.16   16 + 0.25 51 I.H/I.J +Pydiflumetofen A.3.17  16 + 16 96 I.H/I.J + Tebuconazol B.1.25   16 +0.25 54

TABLE I.2 Use examples of fungicidal activity against Botrytis cinereaof I.F as component A and components B Active mixture Code ofConcentration Efficacy (component A + B) component B (ppm) (ppm) I.F +component B A.3.29 4 + 1 87 I.F + component B A.2.5 4 + 1 51 I.F +component B A.3.32 4 + 1 80 I.F + Benomyl D.1.1 4 + 4 100 I.F + BixafenA.3.3   4 + 0.25 58 I.F + Boscalid A.3.4 4 + 4 84 I.F + Captan H.3.4 4 +4 100 I.F + Carbendazim D.1.2   4 + 0.25 100 I.F + Cyproconazol B.1.4 4 + 16 100 I.F + Cyprodinil E.1.1 4 + 4 100 I.F + Dithianon H.4.9 4 + 1100 I.F + Epoxiconazol B.1.8.   4 + 0.25 79 I.F + Fenpropimorph B.2.44 + 1 98 I.F + Fludioxonil F.1.5   4 + 0.25 100 I.F + Fluindapyr A.3.284 + 1 74 I.F + Fluquinconazol B.1.10 4 + 1 100 I.F + component B A.3.244 + 1 82

TABLE I.3 Use examples of fungicidal activity against Botrytis cinereaof I.B/I.C as component A and components B Active mixture Code ofConcentration Efficacy (component A + B) component B (ppm) (ppm)I.B/I.C + component B A.3.29 1 + 1 86 I.B/I.C + component B K.1.29  1 +16 100 I.B/I.C + component B A.2.5 1 + 1 62 I.B/I.C + component B A.3.321 + 1 79 I.B/I.C + component B K.1.30 1 + 4 100 I.B/I.C + component BK.1.32 1 + 1 94 I.B/I.C + component B K.1.31 1 + 4 100 I.B/I.C + BenomylD.1.1 1 + 4 100 I.B/I.C + Bixafen A.3.3   1 + 0.25 58 I.B/I.C + BoscalidA.3.4 1 + 4 84 I.B/I.C + Captan H.3.4 1 + 4 100 I.B/I.C + CarbendazimD.1.2   1 + 0.25 100 I.B/I.C + Cyproconazol B.1.4  1 + 16 100 I.B/I.C +Cyprodinil E.1.1 1 + 4 100 I.B/I.C + Dithianon H.4.9 1 + 1 100 I.B/I.C +Epoxiconazol B.1.8.   1 + 0.25 77 I.B/I.C + Fenpropimorph B.2.4 1 + 1 98I.B/I.C + Fludioxonil F.1.5   1 + 0.25 99 I.B/I.C + Fluindapyr A.3.281 + 1 73 I.B/I.C + Pydiflumetofen A.3.17  1 + 16 96 I.B/I.C +Tebuconazol B.1.25   1 + 0.25 57

TABLE I.4 Use examples fungicidal activity against Botrytis cinerea ofselected components B Code of Common name Concentration Observedcomponent B component B (ppm) efficacy A.3.29 0.25 55 A.2.3 1 11 0.25 0A.2.5 1 6 A.3.34 1 51 0.25 1 A.3.32 0.25 32 K.1.31 1 53 A.1.34 63 18 162 C.1.2 Benalaxyl-M 4 7 D.1.1 Benomyl 0.016 8 A.3.2 Benzovindiflupyr0.063 27 A.3.3 Bixafen 0.25 53 0.063 10 H.3.4 Captan 1 73 0.25 20 H.3.2Chlorothalonil 1 22 E.1.1 Cyprodinil 1 66 A.1.4 Dimoxystrobin 1 14 0.252 B.2.6 Fenpropidin 4 28 B.2.4 Fenpropimorph 0.25 29 F.1.5 Fludioxonil0.016 77 A.3.28 Fluindapyr 0.25 21 H.3.5 Folpet 1 13 A.3.24 0.25 41A.3.29 Isoflucypram 0.25 53 B.1.38 Mefentrifluconazol 0.016 50 A.1.13Picoxystrobin 0.25 9 A.1.14 Pyraclostrobin 0.016 14 0.004 0 A.3.17Pyriofenon 1 2 A.1.17 Trifloxystrobin 0.063 3

TABLE I.5 Use examples of synergistic fungicidal activity againstBotrytis cinerea of compound I.M as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.M 4 — 15 1 — 0 0.25 — 2 0.063 — 1 I.M 1 1:1 33 11 22 A.2.3 1I.M 4 4:1 91 24 67 A.2.3 1 I.M 4 16:1  54 15 39 A.2.3 0.25 I.M 4 4:1 4920 29 A.2.5 1 I.M 4 4:1 77 58 19 A.3.34 1 I.M 4 16:1  41 15 26 A.3.340.25 I.M 1  1:63 55 19 36 A.1.34 63 I.M 4 1:4 99 16 83 A.1.34 16 I.M 11:4 99 7 92 Benalaxyl-M 4 I.M 4  1:63 59 37 22 Benzovindiflupyr 0.063I.M 4 16:1  84 60 24 Bixafen 0.25 I.M 0.25 1:1 72 21 51 Captan 0.25 I.M0.25 1:4 100 74 26 Captan 1 I.M 4 4:1 100 77 23 Captan 1 I.M 4 4:1 92 3359 Chlorothalonil 1 I.M 1 1:1 57 22 35 Chlorothalonil 1 I.M 4 4:1 88 2761 Dimoxystrobin 1 I.M 1 1:1 51 15 36 Dimoxystrobin 1 I.M 4 16:1  50 1634 Dimoxystrobin 0.25 I.M 1 1:4 67 29 38 Fenpropidin 4 I.M 4 1:1 95 3956 Fenpropidin 4 I.M 1 4:1 66 29 37 Fenpropimorph 0.25 I.M 0.063 4:1 9677 19 Fludioxonil 0.016 I.M 4 16:1  54 33 21 Fluindapyr 0.25 I.M 4 16:1 79 60 19 Isoflucypram 0.25 I.M 4 250:1  100 58 42 Mefentrifluconazol0.016 I.M 1 63:1  100 51 49 Mefentrifluconazol 0.016 I.M 4 16:1  70 2248 Picoxystrobin 0.25 I.M 1 4:1 37 9 28 Picoxystrobin 0.25 I.M 4 63:1 40 15 25 Picoxystrobin 0.063 I.M 4 1000:1   57 15 42 Pyraclostrobin0.004 I.M 1 63:1  57 14 43 Pyraclostrobin 0.016 I.M 4 250:1  91 26 65Pyraclostrobin 0.016 I.M 4 63:1  36 17 19 Trifloxystrobin 0.063

TABLE I.6 Use examples of synergistic fungicidal activity againstBotrytis cinerea of compound I.E as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.E 63 — 16 16 — 3 4 — 2 1 — 2 0.063 — 2 I.E 0.063  4:1 33 10 23Benomyl 0.016 I.E 16 250:1  61 35 26 Benzovindiflupyr 0.063 I.E 16 63:181 58 23 Bixafen 0.25 I.E 4 16:1 49 22 27 Captan 0.25 I.E 16 63:1 53 2330 Captan 0.25 I.E 63 63:1 99 71 28 Cyprodinil 1 I.E 16  4:1 63 37 26Fenpropidin 4 I.E 16 63:1 83 31 52 Fenpropimorph 0.25 I.E 4 16:1 56 3026 Fenpropimorph 0.25 I.E 16 16:1 88 16 72 Folpet 1 I.E 63 4000:1  92 5834 Mefentrifluconazol 0.016 I.E 16 1000:1  95 52 43 Mefentrifluconazol0.016

TABLE I.7 Use examples of synergistic fungicidal activity againstBotrytis cinerea of compound I.A as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.A 16 — 12 4 — 1 0.25 — 3 I.A 16 63:1 84 60 24 A.3.29 0.25 I.A16 63:1 49 13 36 A.3.34 0.25 I.A 16 16:1 79 57 22 A.3.34 1 I.A 16 63:172 41 31 A.3.32 0.25 I.A 16 16:1 91 61 30 K.1.31 1 I.A 16  1:1 45 14 31A.1.34 16 I.A 16 250:1  61 35 26 Benzovindiflupyr 0.063 I.A 16 63:1 8158 23 Bixafen 0.25 I.A 16 250:1  54 21 33 Bixafen 0.063 I.A 4  4:1 97 7423 Captan 1 I.A 0.25  1:1 50 23 27 Captan 0.25 I.A 16 16:1 100 77 23Captan 1 I.A 16 16:1 90 70 20 Cyprodinil 1 I.A 16  4:1 63 37 26Fenpropidin 4 I.A 16 63:1 66 31 35 Fluindapyr 0.25 I.A 16 63:1 79 49 30A.3.24 0.25 I.A 16 63:1 82 59 23 Isoflucypram 0.25 I.A 4 250:1  93 51 42Mefentrifluconazol 0.016 I.A 16 250:1  36 16 20 Penthiopyrad 0.063 I.A16 1000:1  59 24 35 Pyraclostrobin 0.016 I.A 4  4:1 23 3 20 Pyriofenon 11) Fungicidal Activity Against Colletaichum orbiculae in theMicrotiterplate Test

The active compounds were formulated separately as a stock solutionhaving a concentration of 10000 ppm in dimethyl sulfoxide. The stocksolutions were mixed according to the ratio, pipetted onto a micro titerplate (MTP) and diluted with water to the stated concentrations. sporesuspension of Colletotrichum orbiculare in an aqueous biomalt oryeast-bactopeptone-sodiumacetate solution was then added. The plateswere placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm daysafter the inoculation. The measured parameters were compared to thegrowth of the active compound-free control variant (100%) and thefungus-free and active compound-free blank value to determine therelative growth in % of the pathogens in the respective activecompounds. These percentages were converted into efficacies.

TABLE II.1 Use examples of fungicidal activity against Colletotrichumorbiculare of I.H/I.J as component A and components B ConcentrationActive mixture Code of A + B Efficacy (component A + B) component B(ppm) (ppm) I.H/I.J + component B A.1.34  16 + 63 82 I.H/I.J + componentB K.1.42 16 + 1 55 I.H/I.J + component B A.1.25    16 + 0.016 53I.H/I.J + component B K.1.53 16 + 1 81 I.H/I.J + component B A.2.3 16 +1 80 I.H/I.J + component B A.2.5 16 + 1 77 I.H/I.J + component B K.1.29 16 + 16 100 I.H/I.J + component B A.3.32 16 + 1 66 I.H/I.J + componentB K.1.30 16 + 4 100 I.H/I.J + component B K.1.32 16 + 1 100 I.H/I.J +component B K.1.31 16 + 4 100 I.H/I.J + Ametoctradin A.4.11  16 + 63 54I.H/I.J + Azoxystrobin A.1.1    16 + 0.063 58 I.H/I.J + Benalaxyl C.1.116 + 4 59 I.H/I.J + Benomyl D.1.1 16 + 4 100 I.H/I.J + BenzovindiflupyrA.3.2    16 + 0.063 88 I.H/I.J + Bixafen A.3.3   16 + 0.25 62 I.H/I.J +Boscalid A.3.4 16 + 4 58 I.H/I.J + Captan H.3.4 16 + 4 99 I.H/I.J +Carbendazim D.1.2   16 + 0.25 99 I.H/I.J + Chlorothalonil H.3.2 16 + 199 I.H/I.J + Cyazofamid A.2.1  16 + 16 83 I.H/I.J + Cyflufenamid K.1.3 16 + 63 57 I.H/I.J + Dimethomorph G.3.1 16 + 4 66 I.H/I.J +Dimoxystrobin A.1.4 16 + 1 67 I.H/I.J + Dithianon H.4.9 16 + 1 100I.H/I.J + Fenpropidin B.2.6 16 + 4 71 I.H/I.J + Fenpropimorph B.2.4 16 +1 60 I.H/I.J + Florylpicoxamid A.2.6 16 + 1 55 I.H/I.J + FludioxonilF.1.5  16 + 97 97 I.H/I.J + Fluopyram A.3.7   16 + 0.25 59 I.H/I.J +Kresoxim-methyl A.1.9 16 + 1 61 I.H/I.J + Mefentrifluconazol B.1.38   16 + 0.016 67 I.H/I.J + Metconazol B.1.17    16 + 0.063 53 I.H/I.J +Metominostrobin A.1.11 16 + 4 71 I.H/I.J + Metrafenone D.2.6  16 + 16 54I.H/I.J + Penthiopyrad A.3.16   16 + 0.25 52 I.H/I.J + PicoxystrobinA.1.13   16 + 0.25 72 I.H/I.J + Pydiflumetofen A.3.17  16 + 16 85I.H/I.J + Pyraclostrobin A.1.14    16 + 0.016 54 I.H/I.J + PyriofenoneA.3.17 16 + 1 66 I.H/I.J + Sulfur H.1.7  16 + 63 100 I.H/I.J +Trifloxystrobin A.1.17    16 + 0.063 57

TABLE II.2 Use examples of fungicidal activity against Colletotrichumorbiculare of I.F as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.F + component B A.1.34  0.016 + 63 83 I.F + component B K.1.53 0.016 +1 76 I.F + component B A.2.3 0.016 + 1 91 I.F + component B A.2.50.016 + 1 82 I.F + component B K.1.29  0.016 + 16 100 I.F + component BK.1.30 0.016 + 4 100 I.F + component B K.1.32 0.016 + 1 100 I.F +component B K.1.31 0.016 + 4 100 I.F + Benomyl D.1.1 0.016 + 4 100 I.F +Benzovindiflupyr A.3.2    0.016 + 0.063 57 I.F + Captan H.3.4 0.016 + 4100 I.F + Carbendazim D.1.2   0.016 + 0.25 100 I.F + ChlorothalonilH.3.2 0.016 + 1 89 I.F + Cyazofamid A.2.1  0.016 + 16 100 I.F +Dimoxystrobin A.1.4 0.016 + 1 71 I.F + Dithianon H.4.9 0.016 + 1 100I.F + Fenpropidin B.2.6 0.016 + 4 61 I.F + Florylpicoxamid A.2.6 0.016 +1 83 I.F + Fludioxonil F.1.5   0.016 + 0.25 100 I.F + FluoxastrobinA.1.8   0.016 + 0.25 62 I.F + Kresoxim-methyl A.1.9 0.016 + 1 80 I.F +Mancozeb H.2.2 0.016 + 1 54 I.F + Metominostrobin A.1.11 0.016 + 4 55I.F + Picoxystrobin A.1.13   0.016 + 0.25 74 I.F + Pydiflumetofen A.3.17 0.016 + 16 92 I.F + Sulfur H.1.7  0.016 + 63 85 I.F + TrifloxystrobinA.1.17    0.016 + 0.063 59

TABLE II.3 Use examples of fungicidal activity against Colletotrichumorbiculare of I.B/I.C as component A and components B ConcentrationActive mixture Code of A + B Efficacy (component A + B) component B(ppm) (ppm) I.B/I.C + component B A.1.34  1 + 63 77 I.B/I.C + componentB K.1.42 1 + 1 69 I.B/I.C + component B A.1.25    1 + 0.016 51 I.B/I.C +component B A.3.29 1 + 1 65 I.B/I.C + component B K.1.53 1 + 1 92I.B/I.C + component B A.2.3 1 + 1 88 I.B/I.C + component B A.2.5 1 + 183 I.B/I.C + component B K.1.29  1 + 16 100 I.B/I.C + component B A.3.321 + 1 57 I.B/I.C + component B K.1.30 1 + 4 100 I.B/I.C + component BK.1.32 1 + 1 100 I.B/I.C + component B K.1.31 1 + 4 100 I.B/I.C +component B K.1.54 1 + 1 67 I.B/I.C + Ametoctradin A.4.11  1 + 63 64I.B/I.C + Azoxystrobin A.1.1    1 + 0.063 65 I.B/I.C + Benalaxyl C.1.11 + 4 56 I.B/I.C + Benalaxyl-M C.1.2 1 + 4 59 I.B/I.C + Benomyl D.1.11 + 4 96 I.B/I.C + Boscalid A.3.4 1 + 4 63 I.B/I.C + Captan H.3.4 1 + 496 I.B/I.C + Carbendazim D.1.2   1 + 0.25 95 I.B/I.C + ChlorothalonilH.3.2 1 + 1 96 I.B/I.C + Cyazofamid A.2.1  1 + 16 95 I.B/I.C +Cyflufenamid K.1.3  1 + 63 79 I.B/I.C + Cyproconazol B.1.4  1 + 16 60I.B/I.C + Difenoconazol B.1.5   1 + 0.25 50 I.B/I.C + Dimethomorph G.3.11 + 4 57 I.B/I.C + Dimoxystrobin A.1.4 1 + 1 75 I.B/I.C + DithianonH.4.9 1 + 1 95 I.B/I.C + Epoxiconazol B.1.8.   1 + 0.25 70 I.B/I.C +Fenpropidin B.2.6 1 + 4 78 I.B/I.C + Florylpicoxamid A.2.6 1 + 1 82I.B/I.C + Fludioxonil F.1.5   1 + 0.25 95 I.B/I.C + Fluindapyr A.3.281 + 1 59 I.B/I.C + Fluopyram A.3.7   1 + 0.25 72 I.B/I.C + FluoxastrobinA.1.8   1 + 0.25 63 I.B/I.C + Fluquinconazol B.1.10 1 + 1 70 I.B/I.C +Fluxapyroxad A.3.9    1 + 0.063 65 I.B/I.C + component B A.3.24 1 + 1 64I.B/I.C + Kresoxim-methyl A.1.9 1 + 1 69 I.B/I.C + Mancozeb H.2.2 1 + 176 I.B/I.C + Mefentrifluconazol B.1.38    1 + 0.016 67 I.B/I.C +Metconazol B.1.17    1 + 0.063 63 I.B/I.C + Metominostrobin A.1.11 1 + 468 I.B/I.C + Penthiopyrad A.3.16   1 + 0.25 70 I.B/I.C + PicoxystrobinA.1.13   1 + 0.25 74 I.B/I.C + Propiconazol B.1.22   1 + 0.25 53I.B/I.C + Prothioconazol B.1.23   1 + 0.25 52 I.B/I.C + PydiflumetofenA.3.17  1 + 16 80 I.B/I.C + Pyriofenone A.3.17 1 + 1 68 I.B/I.C + SulfurH.1.7  1 + 63 100 I.B/I.C + Tebuconazol B.1.25   1 + 0.25 67 I.B/I.C +Trifloxystrobin A.1.17    1 + 0.063 62 I.B/I.C + Triticonazol B.1.29 1 +1 93

TABLE II.4 Use examples fungicidal activity against Colletotrichumorbiculare of selected components B Code of Common name ConcentrationObserved component B component B (ppm) efficacy K.1.42 1 21 0.25 3A.3.29 1 11 A.2.3 0.25 77 0.063 47 A.2.5 0.25 72 A.3.34 1 14 A.3.32 1 15K.1.32 0.25 26 A.1.34 0.000063 37 A.1.25 0.016 13 A.4.11 Ametoctradin 6314 A.1.1 Azoxystrobin 0.016 5 0.004 1 C.1.1 Benalaxyl 4 13 C.1.2Benalaxyl-M 1 2 D.1.1 Benomyl 9 38 A.3.2 Benzovindiflupyr 0.016 3 0.0042 A.3.3 Bixafen 0.063 3 A.3.4 Boscalid 1 0 0.25 0 H.3.4 Captan 0.25 210.001 D.1.2 Carbendazim 0.063 60 K.1.3 Cyflufenamid 16 11 B.1.4Cyproconazol 4 4 E.1.1 Cyprodinil 4 38 1 35 B.1.5 Difenoconazol 0.25 140.016 1 G.3.1 Dimethomorph 4 21 A.1.4 Dimoxystrobin 1 71 H.4.9 Dithianon0.063 21 B.1.8. Epoxiconazol 0.25 17 0.016 2 B.2.6 Fenpropidin 4 47 1 9B.2.4 Fenpropimorph 1 19 0.25 5 F.1.5 Fludioxonil A.3.28 Fluindapyr 1 12A.3.7 Fluopyram 0.25 15 A.1.8 Fluoxastrobin 0.063 51 B.1.10Fluquinconazol 1 12 0.063 3 A.3.9 Fluxapyroxad 0.063 10 0.004 1 H.3.5Folpet 1 20 A.3.24 1 12 0.25 3 A.3.29 Isoflucypram 1 11 0.25 4 A.1.9Kresoxim-methyl 0.25 45 H.2.2 Mancozeb 1 24 0.25 1 B.1.38Mefentrifluconazol 0.016 14 0.001 1 B.1.17 Metconazol 0.063 11 D.2.6Metrafenone 4 14 A.3.16 Penthiopyrad 0.25 8 A.1.13 Picoxystrobin 0.25 630.016 5 B.1.22 Propiconazol 0.25 15 0.016 3 0.063 3 B.1.23Prothioconazol 0.25 14 A.1.14 Pyraclostrobin 0.016 60 0.001 32 B.1.25Tebuconazol 0.25 14 0.063 2 A.1.17 Trifloxystrobin 0.016 9 B.1.29Triticonazol 1 11

TABLE II.5 Use examples of synergistic fungicidal activity againstColletotrichum orbiculare of compound I.M as component A and componentsB Calculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.M 0.016 — 7 0.004 — 1 0.001 — 1 0.00025 — 2 0.000063 — 2 I.M0.016  1:16 30 10 20 K.1.42 0.25 I.M 0.016  1:16 98 79 19 A.2.3 0.25 I.M0.001  1:63 75 48 27 A.2.3 0.063 I.M 0.016  1:16 92 74 18 A.2.5 0.25 I.M0.016  1:16 73 31 42 K.1.32 0.25 I.M 0.000063   1:1000 56 38 18 A.1.340.063 I.M 0.016 1:1 39 17 22 Azoxystrobin 0.016 I.M 0.00025  1:250 70 3931 Benomyl 0.063 I.M 0.000063   1:1000 57 39 18 Benomyl 0.063 I.M 0.001 1:63 70 39 31 Benomyl 0.063 I.M 0.016 1:1 29 10 19 Benzovindiflupyr0.016 I.M 0.016 1:4 30 10 20 Bixafen 0.063 I.M 0.016  1:63 34 8 26Boscalid 1 I.M 0.004  1:63 57 22 35 Captan 0.25 I.M 0.001  1:250 61 2338 Captan 0.25 I.M 0.00025   1:1000 60 23 37 Captan 0.25 I.M 0.016 1:484 63 21 Carbendazim 0.063 I.M 0.016   1:1000 46 18 28 Cyflufenamid 16I.M 0.016 0.08541667 59 40 19 Cyprodinil 1 I.M 0.016  1:250 34 11 23Cyproconazol 4 I.M 0.004   1:4000 76 22 54 Cyproconazol 16 I.M 0.016 1:16 38 20 18 Difenoconazol 0.25 I.M 0.016 1:4 35 7 28 Difenoconazol0.063 I.M 0.016  1:16 67 49 18 Dimoxystrobin 0.25 I.M 0.001  1:63 41 2219 Dithianon 0.063 I.M 0.016 1:4 32 12 20 Epoxiconazol 0.063 I.M 0.016 1:250 77 51 26 Fenpropidin 4 I.M 0.016  1:63 56 15 41 Fenpropidin 1 I.M0.004   1:1000 75 48 27 Fenpropidin 4 I.M 0.016  1:16 57 21 36 Fluopyram0.25 I.M 0.016 1:4 47 9 38 Fluopyram 0.063 I.M 0.016 1:4 33 15 18Fluoxastrobin 0.063 I.M 0.016  1:63 39 19 20 Fluquinconazol 1 I.M 0.016 1:16 42 9 33 Fluquinconazol 0.25 I.M 0.016 1:4 36 17 19 Fluxapyroxad0.063 I.M 0.016 1:1 38 8 30 Fluxapyroxad 0.016 I.M 0.004  1:250 55 21 34Folpet 1 I.M 0.016  1:16 69 49 20 Kresoxim-methyl 0.25 I.M 0.001  1:25063 46 17 Kresoxim-methyl 0.25 I.M 0.016  1:63 56 29 27 Mancozeb 1 I.M0.016  1:16 61 8 53 Mancozeb 0.25 I.M 0.016 4:1 43 8 35Mefentrifluconazol 0.004 I.M 0.016 1:4 42 17 25 Metconazol 0.063 I.M0.016 1:1 36 10 26 Metconazol 0.016 I.M 0.016  1:250 38 20 18Metrafenone 4 I.M 0.016 1:4 35 8 27 Penthiopyrad 0.063 I.M 0.016 1:4 5527 28 Picoxystrobin 0.063 I.M 0.016 1:4 43 10 33 Propiconazol 0.063 I.M0.016 1:4 40 10 30 Prothioconazol 0.063 I.M 0.004 1:4 100 60 40Pyraclostrobin 0.016 I.M 0.004 4:1 75 33 42 Pyraclostrobin 0.001 I.M0.016 1:4 30 9 21 Tebuconazol 0.063 I.M 0.016 1:1 42 15 27Trifloxystrobin 0.016

TABLE II.6 Use examples of synergistic fungicidal activity againstColletotrichum orbiculare of compound I.E as component A and componentsB Calculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A: B efficacy(%) (%) I.E 16 — 52 4 — 11 I.E 1 — 4 0.25 — 4 I.E 16 16:1 84 58 26K.1.42 1 I.E 16 16:1 82 59 23 A.3.32 1 I.E 16 16:1 89 58 31 A.2.5 1 I.E16 16:1 84 57 27 A.3.29 1 I.E 16 1000:1  86 58 28 A.1.25 0.016 I.E 16 1:4 87 58 29 Ametoctradin 63 I.E 16  4:1 87 62 25 Benalaxyl 4 I.E 463:1 90 45 45 Benomyl 0.063 I.E 0.25  4:1 86 41 45 Benomyl 0.063 I.E 1 1:16 86 41 45 Benomyl 0.063 I.E 16 63:1 56 25 31 Captan 0.25 I.E 16250:1  86 65 21 Carbendazim 0.063 I.E 16  4:1 95 62 33 Dimethomorph 4I.E 16 16:1 78 58 20 Fluindapyr 1 I.E 4  4:1 89 29 60 Folpet 1 I.E 1 1:1 65 24 41 Folpet 1 I.E 16 16:1 90 61 29 Folpet 1 I.E 16 63:1 82 5329 A.3.24 0.25 I.E 16 16:1 73 57 16 A.3.24 1 I.E 16 63:1 73 54 19Isoflucypram 0.25 I.E 16 16:1 93 57 36 Isoflucypram 1 I.E 16 63:1 89 5930 Tebuconazol 0.25 I.E 16 250:1  77 53 24 Tebuconazol 0.063 I.E 16 16:180 57 23 Triticonazol 1

TABLE II.7 Use examples of synergistic fungicidal activity againstColletotrichum orbiculare of compound I.A as component A and componentsB Calculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.A 0.063 — 71 0.016 — 2 0.004 — 2 0.001 — 2 0.00025 — 2 I.A0.016 1:63 100 4 96 Benalaxyl-M 1 I.A 0.001 1:63 67 39 28 Benomyl 0.063I.A 0.00025  1:250 70 40 30 Benomyl 0.063 I.A 0.004 1:16 70 39 31Benomyl 0.063 I.A 0.016 1:4  85 61 24 Carbendazim 0.063 I.A 0.016  1:25060 40 20 Cyprodinil 4 I.A 0.016 1:63 55 22 33 Folpet 1 I.A 0.016 16:1 52 33 19 Pyraclostrobin 0.001 I.A 0.016 1:1  96 61 35 Pyraclostrobin0.016 I.A 0.016 1:16 34 16 18 Tebuconazol 0.25111) Fungicidal Activity Against Leptosphaeria nodorum

The active compounds were formulated separately as a stock solutionhaving a concentration of 10000 ppm in dimethyl sulfoxide. The productsulfur was used as a commercial finished formulation and diluted withwater to the stated concentration of the active compound. The stocksolutions were mixed according to the ratio, pipetted onto a microtiterplate (MTP) and diluted with water to the stated concentrations. sporesuspension of Letosphaeria nodorum in an aqueous biomalt oryeast-bactopeptone-sodiumacetate solution was then added. The plateswere placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7days after the inoculation. The measured parameters were compared to thegrowth of the active compound-free control variant (100%) and thefungus-free and active compound-free blank value to determine therelative growth in % of the pathogens in the respective activecompounds. These percentages were converted into efficacies.

TABLE III.1 Use examples of fungicidal activity against Leptosphaerianodorum of I.H/I.J as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) comnponent B (ppm)(ppm) I.H/I.J + component B A.1.34  16 + 63 96 I.H/I.J + component BA.3.29 16 + 1 79 I.H/I.J + component B A.2.3 16 + 1 98 I.H/I.J +component B K.1.29  16 + 16 100 I.H/I.J + component B K.1.30 16 + 4 88I.H/I.J + component B K.1.32 16 + 1 85 I.H/I.J + component B K.1.31 16 +4 94 I.H/I.J + component B K.1.54 16 + 1 58 I.H/I.J + Benomyl D.1.1 16 +4 100 I.H/I.J + Captan H.3.4 16 + 4 100 I.H/I.J + Chlorothalonil H.3.216 + 1 100 I.H/I.J + Cyazofamid A.2.1  16 + 16 88 I.H/I.J + CyproconazolB.1.4  16 + 16 99 I.H/I.J + Cyprodinil E.1.1 16 + 4 100 I.H/I.J +Difenoconazol B.1.5   16 + 0.25 100 I.H/I.J + Diithianon H.4.9 16 + 1100 I.H/I.J + Dimoxystrobin A.1.4 16 + 1 93 I.H/I.J + EpoxiconazolB.1.8.   16 + 0.25 85 I.H/I.J + Fenpropidin B.2.6 16 + 4 64 I.H/I.J +Florylpicoxamid A.2.6 16 + 1 99 I.H/I.J + Fluquinconazol B.1.10 16 + 197 I.H/I.J + Kresoxim-methyl A.1.9 16 + 1 96 I.H/I.J + Metconazol B.1.17   16 + 0.063 58 I.H/I.J + Metominostrobin A.1.11 16 + 4 100 I.H/I.J +Picoxystrobin A.1.13   16 + 0.25 95 I.H/I.J + Propiconazol B.1.22   16 +0.25 63 I.H/I.J + Pydiflumetofen A.3.17  16 + 16 99 I.H/I.J +Pyraclostrobin A.1.14    16 + 0.016 95 I.H/I.J + Sulfur H.1.7  16 + 6393

TABLE III.1 Use examples of fungicidal activity against Leptosphaerianodorum of I. F as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.F + component B A.1.34  4 + 63 100 I.F + component B A.3.29 4 + 1 80I.F + component B A.2.3 4 + 1 100 I.F + component B A.2.5 4 + 1 94 I.F +component B K.1.54 4 + 1 66 I.F + Azoxystrobin A.1.1    4 + 0.063 55I.F + Benomyl D.1.1 4 + 4 99 I.F + Captan H.3.4 4 + 4 100 I.F +Chlorothalonil H.3.2 4 + 1 94 I.F + Cyazofamid A.2.1  4 + 16 63 I.F +Cyproconazol B.1.4  4 + 16 100 I.F + Cyprodinil E.1.1 4 + 4 100 I.F +Difenoconazol B.1.5   4 + 0.25 96 I.F + Dimoxystrobin A.1.4 4 + 1 86I.F + Dithianon H.4.9 4 + 1 100 I.F + Epoxiconazol B.1.8.   4 + 0.25 81I.F + Fenpropidin B.2.6 4 + 4 71 I.F + Fluquinconazol B.1.10 4 + 1 98I.F + Mefentrifluconazol B.1.38    4 + 0.016 54 I.F + Metconazol B.1.17   4 + 0.063 67 I.F + Picoxystrobin A.1.13   4 + 0.25 91 I.F +Propiconazol B.1.22   4 + 0.25 69 I.F + Pyraclostrobin A.1.14    4 +0.016 78 I.F + Tebuconazol B.1.25   4 + 0.25 56

TABLE III.3 Use examples of fungicidal activity against Leptosphaerianodorum of I.B/I.C as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.B/I.C + component B A.1.34  1 + 63 100 I.B/I.C + component B A.3.291 + 1 80 I.B/I.C + component B A.2.3 1 + 1 100 I.B/I.C + component BA.2.5 1 + 1 99 I.B/I.C + component B K.1.29  1 + 16 100 I.B/I.C +component B K.1.30 1 + 4 86 I.B/I.C + component B K.1.32 1 + 1 82I.B/I.C + component B K.1.31 1 + 4 91 I.B/I.C + component B K.1.54 1 + 162 I.B/I.C + Benomyl D.1.1 1 + 4 99 I.B/I.C + Captan H.3.4 1 + 4 100I.B/I.C + Chlorothalonil H.3.2 1 + 1 96 I.B/I.C + Cyazofamid A.2.1  1 +16 65 I.B/I.C + Cyproconazol B.1.4  1 + 16 100 I.B/I.C + CyprodinilE.1.1 1 + 4 100 I.B/I.C + Difenoconazol B.1.5   1 + 0.25 99 I.B/I.C +Dimoxystrobin A.1.4 1 + 1 97 I.B/I.C + Dithianon H.4.9 1 + 1 100I.B/I.C + Epoxiconazol B.1.8.   1 + 0.25 87 I.B/I.C + Fenpropidin B.2.61 + 4 69 I.B/I.C + Florylpicoxamid A.2.6 1 + 1 100 I.B/I.C + FludioxonilF.1.5   1 + 0.25 59 I.B/I.C + Fluoxastrobin A.1.8   1 + 0.25 50I.B/I.C + Fluquinconazol B.1.10 1 + 1 99 I.B/I.C + Kresoxim-methyl A.1.91 + 1 100 I.B/I.C + Metconazol B.1.17    1 + 0.063 63 I.B/I.C +Metominostrobin A.1.11 1 + 4 100 I.B/I.C + Picoxystrobin A.1.13   1 +0.25 96 I.B/I.C + Propiconazol B.1.22   1 + 0.25 64 I.B/I.C +Pydiflumetofen A.3.17  1 + 16 100 I.B/I.C + Pyraclostrobin A.1.14    1 +0.016 81 I.B/I.C + Sulfur H.1.7  1 + 63 100

TABLE III.4 Use examples fungicidal activity against Leptosphaerianodorum of selected components B Code of Common name ConcentrationObserved component B component B (ppm) efficacy K.1.32 0.25 40 A.1.340.063 45 A.1.1 Azoxystrobin 0.063 40 D.1.1 Benomyl 1 15 H.3.4 Captan 144 0.25 13 H.3.2 Chlorothalonil 1 72 A.2.1 Cyazofamid 0.25 6 E.1.1Cyprodinil 0.004 71 B.1.5 Difenoconazol 0.063 41 G.3.1 Dimethomorph 4 41B.2.6 Fenpropidin 1 38 A.1.8 Fluoxastrobin 0.25 38 H.3.5 Folpet 1 40B.1.38 Mefentrifluconazol 0.016 73 0.004 53 A.1.11 Metominostrobin 1 43A.1.13 Picoxystrobin 0.063 42 A.1.14 Pyraclostrobin 0.004 59 0.00025 22H.1.7 Sulfur 4 30

TABLE III.5 Use examples of synergistic fungicidal activity againstLeptosphaeria nodorum of compound I.M as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.M 4 — 52 1 — 18 0.25 — 7 0.016 — 5 0.004 — 6 I.M 0.016 1:4 8248 34 A.1.34 0.063 I.M 4 63:1  91 71 20 Azoxystrobin 0.063 I.M 4 4:1 8666 20 Benomyl 1 I.M 4 16:1  100 73 27 Captan 0.25 I.M 1 1:1 100 54 46Captan 1 I.M 0.25 1:4 100 48 52 Captan 1 I.M 1 1:1 98 77 21Chlorothalonil 1 I.M 1 4:1 100 77 23 Cyazofamid 0.25 I.M 0.004 1:1 98 7325 Cyprodinil 0.004 I.M 4 16:1  89 70 19 Fluoxastrobin 0.25 I.M 1 1:1 7851 27 Folpet 1 I.M 4 63:1  93 72 21 Picoxystrobin 0.063 I.M 1 250:1  10066 34 Pyraclostrobin 0.004 I.M 1 1:4 85 42 43 Sulfur 4 I.M 0.25  1:16 6635 31 Sulfur 4

TABLE III.6 Use examples of synergistic fungicidal activity againstLeptosphaeria nodorum of compound I.E as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.E 63 — 22 16 — 18 I.E 0.25   4:1 94 48 46 A.1.34 0.063 I.E 63 250:1 95 56 39 Captan 0.25 I.E 63 1000:1 75 54 21 Difenoconazol 0.063I.E 63 4000:1 97 79 18 Mefentrifluconazol 0.016 I.E 16 1000:1 100 79 21Mefentrifluconazol 0.016 I.E 63 16000:1  94 63 31 Mefentrifluconazol0.004 I.E 63  63:1 78 56 22 Metominostrobin 1 I.E 63 16000:1  100 68 32Pyraclostrobin 0.004

TABLE III.7 Use examples of synergistic fungicidal activity againstLeptosphaeria nodorum of compound I.A as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.A 16 — 27 4 — 14 1 — 6 0.063 — 3 I.A 16 63:1 77 56 21 K.1.320.25 I.A 0.063 1:1 73 47 26 A.1.34 0.063 I.A 16 250:1 80 56 24Azoxystrobin 0.063 I.A 16 16:1 75 49 26 Benomyl 1 I.A 1 1:1 97 47 50Captan 1 I.A 16 16:1 100 59 41 Captan 1 I.A 16 16:1 100 79 21Chlorothalonil 1 I.A 4 4:1 98 76 22 Chlorothalonil 1 I.A 16 250:1 79 5722 Difenoconazol 0.063 I.A 4 1:1 100 50 50 Dimethomorph 4 I.A 16 16:1 7355 18 Fenpropidin 1 I.A 16 63:1 85 55 30 Fluoxastrobin 0.25 I.A 1 1:1 7044 26 Folpet 1 I.A 4 4:1 68 49 19 Folpet 1 I.A 4 250:1 100 77 23Mefentrifluconazol 0.016 I.A 16 1000:1 100 80 20 Mefentrifluconazol0.016 I.A 16 4000:1 95 66 29 Mefentrifluconazol 0.004 I.A 16 250:1 82 5824 Picoxystrobin 0.063 I.A 0.25 1000:1 67 24 43 Pyraclostrobin 0.00025I.A 0.063 250:1 68 24 44 Pyraclostrobin 0.00025 I.A 16 400:1 100 70 30Pyraclostrobin 0.004 I.A 1 1:4 52 34 18 Sulfur 4IV) Fungicidal Activity Against Pyricularia oryzae

The active compounds were formulated separately as a stock solutionhaving a concentration of 10000 ppm in dimethyl sulfoxide. The stocksolutions were mixed according to the ratio, pipetted onto a micro titerplate (MTP) and diluted with water to the stated concentrations. A sporesuspension of Pyricularia oryzae in an aqueous biomalt oryeast-bactopeptone-sodiumacetate solution was then added. The plateswere placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7days after the inoculation. The measured parameters were compared to thegrowth of the active compound-free control variant (100%) and thefungus-free and active compound-free blank value to determine therelative growth in % of the pathogens in the respective activecompounds. These percentages were converted into efficacies.

TABLE IV.1 Use examples of fungicidal activity against Pyriculariaoryzae of I.H/I.J as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.H/I.J + component B A.1.34  16 + 63 95 I.H/I.J + component B A.1.25   16 + 0.016 64 I.H/I.J + component B A.2.3 16 + 1 98 I.H/I.J +component B A.2.5 16 + 1 97 I.H/I.J + component B K.1.29  16 + 16 99I.H/I.J + component B A.3.34 16 + 1 99 I.H/I.J + component B K.1.30 16 +4 99 I.H/I.J + component B K.1.32 16 + 1 100 I.H/I.J + component BK.1.31 16 + 4 100 I.H/I.J + Azoxystrobin A.1.1    16 + 0.063 89I.H/I.J + Benomyl D.1.1 16 + 4 100 I.H/I.J + Benzovindiflupyr A.3.2   16 + 0.063 98 I.H/I.J + Captan H.3.4 16 + 4 100 I.H/I.J + CarbendazimD.1.2   16 + 0.25 100 I.H/I.J + Chlorothalonil H.3.2 16 + 1 99 I.H/I.J +Cyazofamid A.2.1  16 + 16 96 I.H/I.J + Cyflufenamid K.1.3  16 + 63 69I.H/I.J + Cyproconazol B.1.4  16 + 16 99 I.H/I.J + Cyprodinil E.1.1 16 +4 80 I.H/I.J + Dimoxystrobin A.1.4 16 + 1 94 I.H/I.J + Dithianon H.4.916 + 1 98 I.H/I.J + Florylpicoxamid A.2.6 16 + 1 92 I.H/I.J +Fludioxonil F.1.5   16 + 0.25 68 I.H/I.J + Fluoxastrobin A.1.8   16 +0.25 81 I.H/I.J + component B A.3.24 16 + 1 80 I.H/I.J + Kresoxim-methylA.1.9 16 + 1 61 I.H/I.J + Metominostrobin A.1.11 16 + 4 88 I.H/I.J +Picoxystrobin A.1.13   16 + 0.25 93 I.H/I.J + Pydiflumetofen A.3.17 16 + 16 97 I.H/I.J + Pyraclostrobin A.1.14    16 + 0.016 96 I.H/I.J +Sulfur H.1.7  16 + 63 77 I.H/I.J + Trifloxystrobin A.1.17    16 + 0.06397

TABLE IV.2 Use examples of fungicidal activity against Pyriculariaoryzae of I.F as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.F + component B A.1.34 4 + 63 94 I.F + component B A.1.25 4 + 0.016 57I.F + component B A.2.3 4 + 1 98 I.F + component B A.2.5 4 + 1 97 I.F +component B A.3.34 4 + 1 100 I.F + component B A.3.32 4 + 1 60 I.F +Azoxystrobin A.1.1 4 + 0.063 89 I.F + Benomyl D.1.1 4 + 4 100 I.F +Benzovindiflupyr A.3.2 4 + 0.063 99 I.F + Captan H.3.4 4 + 4 100 I.F +Carbendazim D.1.2 4 + 0.25 100 I.F + Chlorothalonil H.3.2 4 + 1 100I.F + Cyazofamid A.2.1 4 + 16 100 I.F + Cyprodinil E.1.1 4 + 4 80 I.F +Dithianon H.4.9 4 + 1 100 I.F + Fludioxonil F.1.5 4 + 0.25 64 I.F +Fluindapyr A.3.28 4 + 1 59 I.F + component B A.3.24 4 + 1 84 I.F +Picoxystrobin A.1.13 4 + 0.25 97 I.F + Pyraclostrobin A.1.14 4 + 0.01697 I.F + Trifloxystrobin A.1.17 4 + 0.063 98

TABLE IV.3 Use examples of fungicidal activity against Pyriculariaoryzae of I.B/I.C as component A and components B Concentration Activemixture Code of A + B Efficacy (component A + B) component B (ppm) (ppm)I.B/I.C + component B A.1.34  1 + 63 98 I.B/I.C + component B A.1.25   1 + 0.016 79 I.B/I.C + component B A.2.3 1 + 1 99 I.B/I.C + componentB A.2.5 1 + 1 98 I.B/I.C + component B K.1.29  1 + 16 100 I.B/I.C +component B K.1.29 1 + 1 100 I.B/I.C + component B A.3.34 1 + 1 57I.B/I.C + component B A.3.32 1 + 4 100 I.B/I.C + component B K.1.30 1 +1 100 I.B/I.C + component B K.1.32 1 + 4 100 I.B/I.C + AzoxystrobinK.1.31    1 + 0.063 96 I.B/I.C + Benomyl D.1.1 1 + 4 100 I.B/I.C +Benzovindiflupyr A.3.2    1 + 0.063 100 I.B/I.C + Captan H.3.4 1 + 4 100I.B/I.C + Carbendazim D.1.2   1 + 0.25 100 I.B/I.C + ChlorothalonilH.3.2 1 + 1 100 I.B/I.C + Cyazofamid A.2.1  1 + 16 100 I.B/I.C +Cyflufenamid K.1.3  1 + 63 100 I.B/I.C + Cyproconazol B.1.4  1 + 16 99I.B/I.C + Cyprodinil E.1.1 1 + 4 86 I.B/I.C + Dimoxystrobin A.1.4 1 + 199 I.B/I.C + Dithianon H.4.9 1 + 1 100 I.B/I.C + Florylpicoxamid A.2.61 + 1 94 I.B/I.C + Fludioxonil F.1.5   1 + 0.25 84 I.B/I.C + FluindapyrA.3.28 1 + 1 54 I.B/I.C + Fluoxastrobin A.1.8   1 + 0.25 94 I.B/I.C +component B A.3.24 1 + 1 90 I.B/I.C + Kresoxim-methyl A.1.9 1 + 1 65I.B/I.C + Metominostrobin A.1.11 1 + 4 88 I.B/I.C + Picoxystrobin A.1.13  1 + 0.25 99 I.B/I.C + Pydiflumetofen A.3.17  1 + 16 100 I.B/I.C +Pyraclostrobin A.1.14    1 + 0.016 99 I.B/I.C + Sulfur H.1.7  1 + 63 100I.B/I.C + Trifloxystrobin A.1.17    1 + 0.063 99

TABLE IV.4 Use examples fungicidal activity against Pyricularia oryzaeof selected components B Code of Common name Concentration Observedcomponent B component B (ppm) efficacy K.1.42 1 9 0.25 5 A.3.29 1 140.25 2 A.2.3 0.063 54 A.2.5 0.063 44 A.3.34 0.25 40 A.3.32 0.25 34K.1.54 1 19 0.25 4 A.1.25 0.016 30 0.004 4 A.4.11 Ametoctradin 63 13 168 A.1.1 Azoxystrobin 0.016 28 C.1.1 Benalaxyl 4 8 1 2 C.1.2 Benalaxyl-M4 12 1 3 D.1.1 Benomyl 0.25 19 A.3.2 Benzovindiflupyr 0.016 70 A.3.4Boscalid 4 5 H.3.4 Captan 1 53 0.25 13 D.1.2 Carbendazim 0.063 3 A.2.1Cyazofamid 4 13 B.1.4 Cyproconazol 0.25 2 E.1.1 Cyprodinil 1 56 G.3.1Dimethomorph 4 8 1 4 A.1.4 Dimoxystrobin 0.016 34 H.4.9 Dithianon 0.2578 B.1.8. Epoxiconazol 0.25 20 B.2.4 Fenpropimorph 1 8 F.1.5 Fludioxonil0.25 61 0.063 45 A.1.8 Fluoxastrobin 0.063 58 H.3.5 Folpet 1 14 A.3.240.25 5 A.3.29 Isoflucypram 1 11 0.25 5 A.1.9 Kresoximmethyl 1 58 0.25 20A.1.11 Metominostrobin 1 59 D.2.6 Metrafenon 16 21 4 5 A.3.16Penthiopyrad 0.25 14 A.1.13 Picoxystrobin 0.063 63 B.1.23 Prothioconazol0.25 11 A.1.14 Pyraclostrobin 0.001 46 B.1.25 Tebuconazol 0.25 20 0.06634 A.1.17 Trifloxystrobin 0.016 27

TABLE IV.5 Use examples of synergistic fungicidal activity againstPyricularia oryzae of compound I.M as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.M 4 — 32 1 — 9 0.25 — 6 0.063 — 5 I.M 4 4:1 72 41 31 A.3.29 1I.M 4 16:1  60 33 27 A.3.29 0.25 I.M 0.25 4:1 78 56 22 A.2.3 0.063 I.M 116:1  77 58 19 A.2.3 0.063 I.M 1 4:1 70 45 25 A.2.5 0.25 I.M 4 16:1  8859 29 A.2.5 0.25 I.M 4 16:1  59 33 26 A.3.32 0.25 I.M 4 4:1 75 45 30K.1.54 1 I.M 4 16:1  65 34 31 K.1.54 0.25 I.M 4 250:1  88 52 36 A.1.250.016 I.M 4 1000:1   80 35 45 A.1.25 0.004 I.M 4 250:1  84 51 33Azoxystrobin 0.016 I.M 4 1:1 66 38 28 Benalaxyl 4 I.M 4 4:1 65 33 32Benalaxyl 1 I.M 4 1:1 81 40 41 Benalaxyl-M 4 I.M 4 4:1 71 34 37Benalaxyl-M 1 I.M 0.25 1:1 97 23 74 Benomyl 0.25 I.M 0.063 1:4 97 23 74Benomyl 0.25 I.M 1 4:1 94 26 68 Benomyl 0.25 I.M 4 1:1 60 36 24 Boscalid4 I.M 1 1:1 100 57 43 Captan 1 I.M 0.25 1:4 100 55 45 Captan 1 I.M 4 4:1100 68 32 Captan 1 I.M 4 63:1  62 34 28 Carbendazim 0.063 I.M 1 1:4 7621 55 Cyazofamid 4 I.M 4 1:1 100 41 59 Cyazofamid 4 I.M 4 4:1 90 70 20Cyprodinil 1 I.M 4 1:1 59 37 22 Dimethomorph 4 I.M 4 4:1 60 34 26Dimethomorph 1 I.M 4 16:1  100 80 20 Dithianon 0.25 I.M 0.25 1:1 98 7919 Dithianon 0.25 I.M 4 16:1  100 74 26 Fludioxonil 0.25 I.M 1 4:1 94 6529 Fludioxonil 0.25 I.M 4 63:1  100 63 37 Fludioxonil 0.063 I.M 4 4:1 7654 22 Fluindapyr 1 I.M 4 63:1  96 71 25 Fluoxastrobin 0.063 I.M 1 1:1 4922 27 Folpet 1 I.M 4 16:1  59 32 27 Fluindapyr 0.25 I.M 4 16:1  62 35 27A.3.24 0.25 I.M 4 4:1 76 39 37 Isoflucypram 1 I.M 4 16:1  65 35 30Isoflucypram 0.25 I.M 4 16:1  97 46 51 Kresoximmethyl 0.25 I.M 4 4:1 10072 28 Kresoximmethyl 1 I.M 1 1:1 88 62 26 Kresoximmethyl 1 I.M 4 1:4 7046 24 Metrafenon 16 I.M 4 1:1 62 36 26 Metrafenon 4 I.M 1  1:16 99 28 71Metrafenon 16 I.M 4 63:1  99 75 24 Picoxystrobin 0.063 I.M 0.25 250:1 96 49 47 Pyraclostrobin 0.001 I.M 0.063 63:1  90 49 41 Pyraclostrobin0.001 I.M 1 1000:1   97 51 46 Pyraclostrobin 0.001 I.M 4 16:1  77 45 32Tebuconazol 0.25 I.M 4 63:1  64 35 29 Tebuconazol 0.063 I.M 1 63:1  5734 23 Trifloxystrobin 0.016 I.M 4 250:1  98 51 47 Trifloxystrobin 0.016

TABLE IV.6 Use examples of synergistic fungicidal activity againstPyricularia oryzae of compound I.E as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.E 63 — 9 16 — 6 4 — 5 1 — 5 I.E 16  250:1 82 48 34 A.2.5 0.063I.E 63  250:1 84 45 39 A.2.5 0.25 I.E 63 4000:1 73 37 36 A.1.25 0.016I.E 63 4000:1 80 35 45 Azoxystrobin 0.016 I.E 4  16:1 74 23 51 Benomyl0.25 I.E 1   4:1 89 23 66 Benomyl 0.25 I.E 16  63:1 91 23 68 Benomyl0.25 I.E 16  16:1 89 56 33 Captan 1 I.E 4   4:1 92 55 37 Captan 1 I.E 63 63:1 100 57 43 Captan 1 I.E 63 1000:1 75 50 25 Fludioxonil 0.063 I.E 631000:1 92 62 30 Fluoxastrobin 0.063 I.E 63  63:1 90 62 28 Kresoximmethyl1 I.E 63  250:1 79 28 51 Kresoximmethyl 0.25 I.E 63 1000:1 86 66 20Picoxystrobin 0.063 I.E 4 4000:1 93 49 44 Pyraclostrobin 0.001 I.E 1616000:1  96 49 47 Pyraclostrobin 0.001 I.E 1 1000:1 93 49 44Pyraclostrobin 0.001 I.E 63 4000:1 88 34 54 Trifloxystrobin 0.016

TABLE IV.7 Use examples of synergistic fungicidal activity againstPyricularia oryzae of compound I.A as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.A 16 — 38 4 — 12 1 — 6 0.25 — 2 I.A 1 16:1 66 48 18 A.2.50.063 I.A 4 16:1 73 47 26 A.2.5 0.25 I.A 1  4:1 66 43 23 A.2.5 0.25 I.A16 63:1 95 62 33 A.2.5 0.25 I.A 16 1000:1  77 56 21 A.1.25 0.016 I.A 4250:1  71 36 35 Azoxystrobin 0.016 I.A 1 63:1 55 32 23 Azoxystrobin0.016 I.A 16 1000:1  96 55 41 Azoxystrobin 0.016 I.A 1  4:1 99 24 75Benomyl 0.25 I.A 0.25  1:1 54 21 33 Benomyl 0.25 I.A 4 16:1 96 28 68Benomyl 0.25 I.A 4 250:1  94 73 21 Benzovindiflupyr 0.016 I.A 16 1000:1 100 81 19 Benzovindiflupyr 0.016 I.A 4 16:1 69 23 46 Captan 0.25 I.A 1 1:1 100 56 44 Captan 1 I.A 4  4:1 100 58 42 Captan 1 I.A 16  4:1 81 4635 Cyazofamid 4 I.A 4 16:1 87 69 18 Cyproconazol 0.25 I.A 4  1:1 86 1967 Dimethomorph 4 I.A 0.25 16:1 57 36 21 Dimoxystrobin 0.016 I.A 16 63:170 50 20 Epoxiconazol 0.25 I.A 4 16:1 51 30 21 Epoxiconazol 0.25 I.A 1616:1 70 42 28 Fenpropimorph 1 I.A 4  4:1 100 18 82 Fenpropimorph 1 I.A 416:1 92 66 26 Fludioxonil 0.25 I.A 4 63:1 81 51 30 Fludioxonil 0.063 I.A16 250:1  94 66 28 Fludioxonil 0.063 I.A 4  4:1 59 40 19 Fluindapyr 1I.A 4 63:1 83 63 20 Fluoxastrobin 0.063 I.A 16 250:1  96 74 22Fluoxastrobin 0.063 I.A 1  1:1 42 20 22 Folpet 1 I.A 4  4:1 51 24 27Folpet 1 I.A 16 16:1 100 74 26 Kresoximmethyl 1 I.A 16 63:1 98 50 48Kresoximmethyl 0.25 I.A 1  4:1 47 25 22 Kresoximmethyl 0.25 I.A 16 16:192 74 18 Metominostrobin 1 I.A 16  1:1 75 51 24 Metrafenon 16 I.A 4 16:149 24 25 Penthiopyrad 0.25 I.A 1 16:1 83 65 18 Picoxystrobin 0.063 I.A16 250:1  99 77 22 Picoxystrobin 0.063 I.A 4 63:1 91 67 24 Picoxystrobin0.063 I.A 16 63:1 62 44 18 Prothioconazol 0.25 I.A 4 4000:1  95 53 42Pyraclostrobin 0.001 I.A 1 1000:1  93 50 43 Pyraclostrobin 0.001 I.A0.25 250:1  89 48 41 Pyraclostrobin 0.001 I.A 16 63:1 72 50 22Tebuconazol 0.25 I.A 4 250:1  65 36 29 Trifloxystrobin 0.016 I.A 4 16:148 29 19 Tebuconazol 0.25 I.A 16 1000: 1  98 55 43 Trifloxystrobin 0.016V) Fungicidal Activity Against Septoria tritici

The active compounds were formulated separately as a stock solutionhaving a concentration of 10000 ppm in dimethyl sulfoxide. The stocksolutions were mixed according to the ratio, pipetted onto a micro titerplate (MTP) and diluted with water to the stated concentrations. A sporesuspension of Septoria tritici in an aqueous biomalt oryeast-bactopeptone-sodiumacetate solution was then added. The plateswere placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7days after the inoculation. The measured parameters were compared to thegrowth of the active compound-free control variant (100%) and thefungus-free and active compound-free blank value to determine therelative growth in % of the pathogens in the respective activecompounds. These percentages were converted into efficacies.

TABLE V.1 Use examples of fungicidal activity against Septoria triticiof I.H/I.J as component A and components B Concentration Active mixtureCode of A + B Efficacy (component A + B) component B (ppm) (ppm)I.H/I.J + component B A.1.34  16 + 63 79 I.H/I.J + Boscalid A.3.4 16 + 4100 I.H/I.J + Chlorothalonil H.3.2 16 + 1 100 I.H/I.J + CyproconazolB.1.4  16 + 16 100 I.H/I.J + Difenoconazol B.1.5   16 + 0.25 96I.H/I.J + Dimoxystrobin A.1.4 16 + 1 97 I.H/I.J + Epoxiconazol B.1.8.  16 + 0.25 96 I.H/I.J + Fenpropidin B.2.6 16 + 4 96 I.H/I.J +Florylpicoxamid A.2.6 16 + 1 90 I.H/I.J + Kresoxim-methyl A.1.9 16 + 190 I.H/I.J + Pydiflumetofen A.3.17  16 + 16 91 I.H/I.J + Sulfur H.1.7 16 + 63 96 I.H/I.J + Triticonazol B.1.29 16 + 1 92

TABLE V.2 Use examples of fungicidal activity against Septoria triticiof I.F as component A and components B Concentration Active mixture Codeof A + B Efficacy (component A + B) component B (ppm) (ppm) I.F +component B A.1.34  4 + 63 100 I.F + component B A.1.25    4 + 0.016 75I.F + component B A.3.29 4 + 1 100 I.F + component B A.3.34 4 + 1 96I.F + component B A.3.32 4 + 1 98 I.F + Azoxystrobin A.1.1    4 + 0.06353 I.F + Benzovindiflupyr A.3.2    4 + 0.063 54 I.F + Bixafen A.3.3  4 + 0.25 72 I.F + Boscalid A.3.4 4 + 4 96 I.F + Captan H.3.4 4 + 4 100I.F + Chlorothalonil H.3.2 4 + 1 99 I.F + Cyazofamid A.2.1  4 + 16 61I.F + Cyproconazol B.1.4  4 + 16 93 I.F + Difenoconazol B.1.5   4 + 0.2592 I.F + Dimoxystrobin A. 1.4 4 + 1 100 I.F + Dithianon H.4.9 4 + 1 100I.F + Epoxiconazol B.1.8.   4 + 0.25 91 I.F + Fluindapyr A.3.28 4 + 1 91I.F + Fluquinconazol B.1.10 4 + 1 94 I.F + component B A.3.24 4 + 1 98I.F + Mefentrifluconazol B.1.38    4 + 0.016 94 I.F + Metconazol B.1.17   4 + 0.063 77 I.F + Penthiopyrad A.3.16   4 + 0.25 88 I.F +Picoxystrobin A.1.13   4 + 0.25 100 I.F + Propiconazol B.1.22   4 + 0.2585 I.F + Prothioconazol B.1.23   4 + 0.25 85 I.F + Pyraclostrobin A.1.14   4 + 0.016 100 I.F + Trifloxystrobin A.1.17    4 + 0.063 100 I.F +Triticonazol B.1.29 4 + 1 95

TABLE V.3 Use examples of fungicidal activity against Septoria triticiof I.B/I.C as component A and components B Concentration Active mixtureCode of A + B Efficacy (component A + B) component B (ppm) (ppm)I.B/I.C + component B A.1.34  1 + 63 100 I.B/I.C + component B A.1.25   1 + 0.016 53 I.B/I.C + component B A.3.29 1 + 1 100 I.B/I.C +component B A.2.3 1 + 1 100 I.B/I.C + component B A.2.5 1 + 1 100I.B/I.C + component B K.1.29  1 + 16 99 I.B/I.C + component B A.3.34 1 +1 100 I.B/I.C + component B A.3.32 1 + 1 99 I.B/I.C + Azoxystrobin A.1.1   1 + 0.063 99 I.B/I.C + Benzovindiflupyr A.3.2    1 + 0.063 96I.B/I.C + Bixafen A.3.3   1 + 0.25 98 I.B/I.C + Boscalid A.3.4 1 + 4 99I.B/I.C + Captan H.3.4 1 + 4 100 I.B/I.C + Chlorothalonil H.3.2 1 + 1 99I.B/I.C + Cyazofamid A.2.1  1 + 16 50 I.B/I.C + Cyflufenamid K.1.3  1 +63 52 I.B/I.C + Cyproconazol B.1.4  1 + 16 99 I.B/I.C + DifenoconazolB.1.5   1 + 0.25 100 I.B/I.C + Dimoxystrobin A.1.4 1 + 1 100 I.B/I.C +Dithianon H.4.9 1 + 1 99 I.B/I.C + Epoxiconazol B.1.8.   1 + 0.25 100I.B/I.C + Fenpropidin B.2.6 1 + 4 100 I.B/I.C + Fenpropimorph B.2.4 1 +1 82 I.B/I.C + Florylpicoxamid A.2.6 1 + 1 100 I.B/I.C + FluindapyrA.3.28 1 + 1 94 I.B/I.C + Fluopyram A.3.7   1 + 0.25 79 I.B/I.C +Fluquinconazol B.1.10 1 + 1 100 I.B/I.C + Fluxapyroxad A.3.9    1 +0.063 83 I.B/I.C + component B A.3.24 1 + 1 95 I.B/I.C + Kresoxim-methylA.1.9 1 + 1 99 I.B/I.C + Mefentrifluconazol B.1.38    1 + 0.016 100I.B/I.C + Metconazol B.1.17    1 + 0.063 98 I.B/I.C + PenthiopyradA.3.16   1 + 0.25 97 I.B/I.C + Picoxystrobin A.1.13   1 + 0.25 98I.B/I.C + Propiconazol B.1.22   1 + 0.25 100 I.B/I.C + ProthioconazolB.1.23   1 + 0.25 99 I.B/I.C + Pydiflumetofen A.3.17  1 + 16 100I.B/I.C + Pyraclostrobin A.1.14    1 + 0.016 100 I.B/I.C + Sulfur H.1.7 1 + 63 100 I.B/I.C + Tebuconazol B.1.25   1 + 0.25 96 I.B/I.C +Trifloxystrobin A.1.17    1 + 0.063 100 I.B/I.C + Triticonazol B.1.291 + 1 97

TABLE V.4 Use examples fungicidal activity against Septoria tritici ofselected components B Code of Common name Concentration Observedcomponent B component B (ppm) efficacy A.3.29 0.063 68 A.2.3 0.016 52A.2.5 0.063 33 K.1.29 4 6 A.3.34 0.25 17 A.3.32 1 70 0.25 22 K.1.30 4 01 0 K.1.32 1 0 0.25 0 K.1.31 4 62 1 5 K.1.54 1 3 A.1.25 0.016 25 0.004 3A.1.1 Azoxystrobin 0.063 28 0.016 4 A.3.2 Benzovindiflupyr 0.063 350.016 17 A.3.3 Bixafen 0.25 41 0.063 16 A.3.4 Boscalid 1 61 H.3.4 Captan0.25 22 H.3.2 Chlorothalonil 0.25 25 A.2.1 Cyazofamid 16 8 4 2 B.1.5Difenoconazol 0.016 4 G.3.1 Dimethomorph 4 11 A.1.4 Dimoxystrobin 0.06335 B.1.8. Epoxiconazol 0.063 52 B.2.6 Fenpropidin 1 1 B.2.4Fenpropimorph 0.25 0 A.2.6 Florylpicoxamid 0.25 68 F.1.5 Fludioxonil0.063 5 A.3.28 Fluindapyr 1 58 0.25 21 A.3.7 Fluopyram 0.25 33 0.063 13A.1.8 Fluoxastrobin 0.25 32 0.063 3 A.3.9 Fluxapyroxad 0.063 10 0.016 12H.3.5 Folpet 1 70 A.3.24 1 76 0.25 25 A.3.29 Isoflucypram 1 62 0.25 61A.1.9 Kresoximmethyl 0.063 41 H.2.2 Mancozeb 1 9 0.25 7 B.1.38Mefentrifluconazol 0.00025 6 A.1.11 Metominostrobin 1 46 D.2.6Metrafenon 16 1 4 1 A.3.16 Penthiopyrad 0.25 28 0.063 5 A.1.13Picoxystrobin 0.063 34 B.1.22 Propiconazol 0.063 17 A.1.14Pyraclostrobin 0.000063 21 A.1.17 Trifloxystrobin 0.016 43

TABLE V.5 Use examples of synergistic fungicidal activity againstSeptoria tritici of compound I.M as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.M 4 — 42 1 — 35 0.25 — 23 0.063 — 14 I.M 1 16:1 94 76 18A.3.29 0.063 I.M 4  1:1 70 46 24 K.1.29 4 I.M 1  1:4 57 30 27 K.1.29 4I.M 4 16:1 96 52 44 A.2.5 0.25 I.M 1  4:1 73 38 35 A.2.5 0.25 I.M 1  1:196 78 18 A.3.32 1 I.M 4 16:1 90 55 35 A.3.32 0.25 I.M 1  1:1 52 29 23K.1.31 1 I.M 4 250:1  100 57 43 A.1.25 0.016 I.M 4 1000:1  90 44 46A.1.25 0.004 I.M 4 63:1 100 58 42 Azoxystrobin 0.063 I.M 1 16:1 82 46 36Azoxystrobin 0.063 I.M 4 250:1  90 45 45 Azoxystrobin 0.016 I.M 4 63:198 63 35 Benzovindiflupyr 0.063 I.M 1 16:1 85 52 33 Benzovindiflupyr0.063 I.M 4 250:1  82 52 30 Benzovindiflupyr 0.016 I.M 4 16:1 99 66 33Bixafen 0.25 I.M 1  4:1 93 56 37 Bixafen 0.25 I.M 4 63:1 91 52 39Bixafen 0.063 I.M 1  1:1 100 71 29 Boscalid 1 I.M 4  4:1 100 77 23Boscalid 1 I.M 0.25  1:4 97 70 27 Boscalid 1 I.M 1  4:1 100 44 56Chlorothalonil 0.25 I.M 4 16:1 100 56 44 Chlorothalonil 0.25 I.M 4  1:498 47 51 Cyazofamid 16 I.M 1  1:16 59 31 28 Cyazofamid 16 I.M 1 16:1 9052 38 Dimoxystrobin 0.063 I.M 4 63:1 96 72 24 Epoxiconazol 0.063 I.M 4 4:1 61 43 18 Fenpropidin 1 I.M 4 16:1 62 42 20 Fenpropimorph 0.25 I.M 1 4:1 94 76 18 Florylpicoxamid 0.25 I.M 4 16:1 100 82 18 Florylpicoxamid0.25 I.M 1 16:1 50 30 20 Fludioxonil 0.063 I.M 4  4:1 99 76 23Fluindapyr 1 I.M 4 16:1 85 54 31 Fluindapyr 0.25 I.M 1  1:1 92 68 24Fluindapyr 1 I.M 4 63:1 70 50 20 Fluopyram 0.063 I.M 4 16:1 96 61 35Fluopyram 0.25 I.M 1  4:1 68 50 18 Fluopyram 0.25 I.M 4 63:1 83 44 39Fluoxastrobin 0.063 I.M 4 16:1 100 61 39 Fluoxastrobin 0.25 I.M 1  4:168 50 18 Fluoxastrobin 0.25 I.M 4 63:1 87 48 39 Fluxapyroxad 0.063 I.M 4250:1  67 49 18 Fluxapyroxad 0.016 I.M 1  1:1 99 78 21 Folpet 1 I.M 0.25 1:4 97 77 20 Folpet 1 I.M 4 16:1 95 57 38 A.3.24 0.25 I.M 4 16:1 100 7723 Isoflucypram 0.25 I.M 1  1:1 100 71 29 Isoflucypram 1 I.M 4 16:1 7247 25 Mancozeb 0.25 I.M 4  4:1 82 47 35 Mancozeb 1 I.M 0.063 250:1  5119 32 Mefentrifluconazol 0.00025 I.M 4  4:1 99 69 30 Metominostrobin 1I.M 1  1:16 50 26 24 Metrafenon 16 I.M 4 16:1 98 59 39 Penthiopyrad 0.25I.M 1  4:1 98 47 51 Penthiopyrad 0.25 I.M 4 63:1 92 45 47 Penthiopyrad0.063 I.M 4 63:1 100 62 38 Picoxystrobin 0.063 I.M 1 16:1 98 51 47Picoxystrobin 0.063 I.M 0.25  4:1 91 49 42 Picoxystrobin 0.063 I.M 116:1 57 38 19 Propiconazol 0.063 I.M 1 63:1 89 58 31 Trifloxystrobin0.016 I.M 4 250:1  100 67 33 Trifloxystrobin 0.016

TABLE V.6 Use examples of synergistic fungicidal activity againstSeptoria tritici of compound I.E as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.E 63 — 14 16 — 13 4 — 7 0.25 — 13 I.E 4 63:1 62 38 24 A.2.50.063 I.E 16 250:1  59 37 22 Azoxystrobin 0.063 I.E 16 63:1 54 32 22Captan 0.25 I.E 63 16:1 78 15 63 Cyazofamid 4 I.E 16 16:1 84 63 21Fluindapyr 1 I.E 63 63:1 92 67 25 Isoflucypram 1 I.E 16 16:1 97 66 31Isoflucypram 1 I.E 63 250:1  98 66 32 Isoflucypram 0.25 I.E 0.25 4000:1 57 32 25 Pyraclostrobin 0.000063

TABLE V.7 Use examples of synergistic fungicidal activity againstSeptoria tritici of compound I.E as component A and components BCalculated Active efficacy compound/ Concen- according Syner- activemixture tration Ratio Observed to Colby gism A + B (ppm) A:B efficacy(%) (%) I.A 16 — 19 4 — 8 1 — 0 0.25 — 2 0.063 — 3 I.A 1 16:1 95 68 27A.3.29 0.063 I.A 0.25 16:1 91 53 38 A.2.3 0.016 I.A 1 16:1 100 34 66A.2.5 0.063 I.A 4  1:1 79 13 66 K.1.29 4 I.A 1  1:4 53 6 47 K.1.29 4 I.A16  4:1 92 24 68 K.1.29 4 I.A 4 16:1 82 23 59 A.2.5 0.25 I.A 1  4:1 5517 38 A.2.5 0.25 I.A 16 63:1 85 33 52 A.2.5 0.25 I.A 16 16:1 100 76 24A.3.32 1 I.A 4  4:1 94 73 21 A.3.32 1 I.A 16 63:1 79 37 42 A.3.32 0.25I.A 4  1:1 27 8 19 K.1.30 4 I.A 16 16:1 37 19 18 K.1.30 1 I.A 4  4:1 298 21 K.1.32 1 I.A 16 63:1 41 19 22 K.1.32 0.25 I.A 16  4:1 100 70 30K.1.31 4 I.A 4  1:1 90 65 25 K.1.31 4 I.A 16 16:1 45 24 21 K.1.31 1 I.A4  4:1 99 10 89 K.1.54 1 I.A 16 1000:1  99 39 60 A.1.25 0.016 I.A 4250:1  57 31 26 A.1.25 0.016 I.A 16 4000:1  41 22 19 A.1.25 0.004 I.A 16250:1  99 42 57 Azoxystrobin 0.063 I.A 4 63:1 70 33 37 Azoxystrobin0.063 I.A 16 1000:1  75 23 52 Azoxystrobin 0.016 I.A 16 250:1  94 48 46Benzovindiflupyr 0.063 I.A 16 1000:1  61 33 28 Benzovindiflupyr 0.016I.A 4 63:1 73 40 33 Benzovindiflupyr 0.063 I.A 16 63:1 100 53 47 Bixafen0.25 I.A 16 250:1  85 33 52 Bixafen 0.063 I.A 4 16:1 90 46 44 Bixafen0.25 I.A 4  4:1 100 64 36 Boscalid 1 I.A 1  1:1 97 61 36 Boscalid 1 I.A16 16:1 97 69 28 Boscalid 1 I.A 4 16:1 100 30 70 Chlorothalonil 0.25 I.A1  4:1 76 25 51 Chlorothalonil 0.25 I.A 16 63:1 98 39 59 Chlorothalonil0.25 I.A 16  1:1 51 26 25 Cyazofamid 16 I.A 4 250:1  57 12 45Difenoconazol 0.016 I.A 1 16:1 46 4 42 Difenoconazol 0.063 I.A 4  1:1 5618 38 Dimethomorph 4 I.A 1 16:1 97 35 62 Dimoxystrobin 0.063 I.A 4 63:192 40 52 Dimoxystrobin 0.063 I.A 16 250:1  93 62 31 Epoxiconazol 0.063I.A 4 63:1 82 56 26 Epoxiconazol 0.063 I.A 4 16:1 99 71 28Florylpicoxamid 0.25 I.A 16 63:1 100 75 25 Florylpicoxamid 0.25 I.A 463:1 43 13 30 Fludioxonil 0.063 I.A 1 16:1 29 6 23 Fludioxonil 0.063 I.A16 16:1 100 66 34 Fluindapyr 1 I.A 4  4:1 87 61 26 Fluindapyr 1 I.A 1663:1 55 36 19 Fluindapyr 0.25 I.A 16 63:1 84 46 38 Fluopyram 0.25 I.A 416:1 65 38 27 Fluopyram 0.25 I.A 16 63:1 100 46 54 Fluoxastrobin 0.25I.A 4 16:1 77 38 39 Fluoxastrobin 0.25 I.A 16 250:1  76 22 54Fluoxastrobin 0.063 I.A 4 63:1 53 17 36 Fluxapyroxad 0.063 I.A 16 250:1 63 28 35 Fluxapyroxad 0.063 I.A 1  1:1 100 70 30 Folpet 1 I.A 4  4:1 10072 28 Folpet 1 I.A 16 63:1 87 40 47 A.3.24 0.25 I.A 16 16:1 100 81 19A.3.24 1 I.A 1  4:1 55 25 30 A.3.24 0.25 I.A 4 16:1 100 64 36Isoflucypram 0.25 I.A 16 63:1 100 68 32 Isoflucypram 0.25 I.A 1 16:1 9141 50 Kresoximmethyl 0.063 I.A 4 63:1 99 46 53 Kresoximmethyl 0.063 I.A16 63:1 44 25 19 Mancozeb 0.25 I.A 0.25 1000:1  48 8 40Mefentrifluconazol 0.00025 I.A 1 4000:1  43 6 37 Mefentrifluconazol0.00025 I.A 4  4:1 91 51 40 Metominostrobin 1 I.A 16 16:1 100 57 43Metominostrobin 1 I.A 16  1:1 72 20 52 Metrafenon 16 I.A 4  1:4 78 8 70Metrafenon 16 I.A 16  4:1 60 20 40 Metrafenon 4 I.A 4 16:1 93 34 59Penthiopyrad 0.25 I.A 16 250:1  78 24 54 Penthiopyrad 0.063 I.A 16 63:197 42 55 Penthiopyrad 0.25 I.A 4 63:1 94 39 55 Picoxystrobin 0.063 I.A16 250:1  100 47 53 Picoxystrobin 0.063 I.A 16 250:1  54 33 21Propiconazol 0.063 I.A 1 16:1 40 17 23 Propiconazol 0.063 I.A 0.0631000:1  91 23 68 Pyraclostrobin 0.000063 I.A 4 250:1  100 48 52Trifloxystrobin 0.016 I.A 16 1000:1  99 54 45 Trifloxystrobin 0.016

1-10. (canceled) 11: A fungicidal mixture comprising as activecomponents 1) at least one active compound of the formula I, or anN-oxide, or an agriculturally useful salt thereof,

wherein: W is —(C═O)—NR²-#, —(C═S)—NR²-#, —NR²—(C═O)-# or —NR²—(C═S)-#;wherein # denotes the position, which is attached to the group R¹; R¹ isC₁-C₆-alkyl, C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₆-alkoxyimino-C₁-C₄-alkyl or phenyl; wherein thephenyl ring is unsubstituted or substituted with 1, 2, 3 or up to themaximum possible number of identical or different radicals selected fromthe group consisting of halogen, C₁-C₆-alkyl and C₁-C₆-alkoxy; R² ishydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxy,C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, and C₃-C₈-cycloalkyl-C₁-C₄-alkyl;and wherein any of the aliphatic or cyclic groups are unsubstituted orsubstituted with 1, 2, 3 or up to the maximum possible number ofidentical or different radicals selected from the group consisting ofhalogen, hydroxy, oxo, cyano, C₁-C₆-alkyl, C₁-C₆-alkoxy andC₃-C₈-cycloalkyl; or R¹ and R² together with the nitrogen atom to whichthey are bound form a saturated or partially unsaturated mono- orbicyclic 3- to 7-membered heterocycle, wherein the heterocycle includesbeside one nitrogen atom and one or more carbon atoms no furtherheteroatom or 1, 2 or 3 further heteroatoms independently selected fromN, O and S as ring member atoms; and wherein one or two CH₂ groups ofthe heterocycle may be replaced by one or two groups independentlyselected from the group of C(═O) and C(═S); and wherein the heterocycleis unsubstituted or carries 1, 2, 3, 4 or up to the maximum possiblenumber of identical or different radicals selected from the groupconsisting of halogen, cyano, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₁-C₆-alkoxy, m is 0 or 1; R³, R⁴ independently of each other areselected from the group consisting of hydrogen, halogen, cyano,C₁-C₄-alkyl, C₁-C₄-alkenyl, C₁-C₄-alkynyl, C₁-C₄-haloalkyl andC₁-C₄-alkoxy; or R³ and R⁴ together with the carbon atom to which theyare bound form a cyclopropyl ring; and as component 2) at least oneactive compound II selected from groups A) to O), or an N-oxide, or anagriculturally useful salt thereof: A) Respiration inhibitors:Inhibitors of complex III at Q_(o) site: azoxystrobin (A.1.1),coumethoxystrobin (A.1.2), coumoxystrobin (A.1.3), dimoxystrobin(A.1.4), enestroburin (A.1.5), fenaminstrobin (A.1.6),fenoxystrobin/flufenoxystrobin (A.1.7), fluoxastrobin (A.1.8),kresoxim-methyl (A.1.9), mandestrobin (A.1.10), metominostrobin(A.1.11), orysastrobin (A.1.12), picoxystrobin (A.1.13), pyraclostrobin(A.1.14), pyrametostrobin (A.1.15), pyraoxystrobin (A.1.16),trifloxystrobin (A.1.17),2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymethyl)-phenyl)-2-methoxyimino-N-methyl-acetamide(A.1.18), pyribencarb (A.1.19), triclopyricarb/chlorodincarb (A.1.20),famoxadone (A.1.21), fenamidone (A.1.21a),methyl-N-[2-[(1,4-dimethyl-5-phenyl-pyrazol-3-yl)oxylmethyl]phenyl]-N-methoxy-carbamate(A.1.22),1-[3-chloro-2-[[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.23),1-[3-bromo-2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.24),1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one(A.1.25),1-[2-[[1-(4-chlorophenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one(A.1.26),1-[2-[[1-(2,4-dichloro-phenyl)pyrazol-3-yl]oxymethyl]-3-fluoro-phenyl]-4-methyl-tetrazol-5-one(A.1.27),1-[2-[[4-(4-chlorophenyl)thiazol-2-yl]oxymethyl]-3-methyl-phenyl]-4-methyl-tetrazol-5-one(A.1.28),1-[3-chloro-2-[[4-(p-tolyl)thiazol-2-yl]oxymethyl]phenyl]-4-methyl-tetrazol-5-one(A.1.29),1-[3-cyclopropyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one(A.1.30),1-[3-(difluoromethoxy)-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]-4-methyl-tetrazol-5-one(A.1.31),1-methyl-4-[3-methyl-2-[[2-methyl-4-(1-methylpyrazol-3-yl)phenoxy]methyl]phenyl]tetrazol-5-one(A.1.32),1-methyl-4-[3-methyl-2-[[1-[3-(trifluoromethyl)phenyl]-ethylideneamino]oxymethyl]phenyl]tetrazol-5-one(A.1.33),(Z,2E)-5-[1-(2,4-dichlorophenyl)pyrazol-3-yl]-oxy-2-methoxyimino-N,3-dimethyl-pent-3-enamide(A.1.34),(Z,2E)-5-[1-(4-chlorophenyl)pyrazol-3-yl]oxy-2-methoxyimino-N,3-dimethyl-pent-3-enamide(A.1.35), pyriminostrobin (A.1.36), bifujunzhi (A.1.37),2-(ortho-((2,5-dimethylphenyl-oxymethylen)phenyl)-3-methoxy-acrylic acidmethylester (A.1.38); Inhibitors of complex III at Q_(i) site:cyazofamid (A.2.1), amisulbrom (A.2.2),[(6S,7R,8R)-8-benzyl-3-[(3-hydroxy-4-methoxy-pyridine-2-carbonyl)amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]2-methylpropanoate (A.2.3), fenpicoxamid (A.2.4),[(6S,7R,8R)-8-benzyl-3-[[4-methoxy-3-(propanoyloxymethoxy)pyridine-2-carbonyl]amino]-6-methyl-4,9-dioxo-1,5-dioxonan-7-yl]2-methylpropanoate (A.2.5), florylpicoxamid (A.2.6); Inhibitors ofcomplex II benodanil (A.3.1), benzovindiflupyr (A.3.2), bixafen (A.3.3),boscalid (A.3.4), carboxin (A.3.5), fenfuram (A.3.6), fluopyram (A.3.7),flutolanil (A.3.8), fluxapyroxad (A.3.9), furametpyr (A.3.10),isofetamid (A.3.11), isopyrazam (A.3.12), mepronil (A.3.13), oxycarboxin(A.3.14), penflufen (A.3.15), penthiopyrad (A.3.16), pydiflumetofen(A.3.17),N-[2-(3,4-difluorophenyl)phenyl]-3-(trifluoromethyl)pyrazine-2-carboxamide(A.3.18), sedaxane (A.3.19), tecloftalam (A.3.20), thifluzamide(A.3.21),3-(difluoromethyl)-1-methyl-N-(1,1,3-trimethyl-indan-4-yl)pyrazole-4-carboxamide(A.3.22),3-(trifluoromethyl)-1-methyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.23),1,3-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.24),3-(trifluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.25),1,3,5-trimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.26),3-(difluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindan-4-yl)pyrazole-4-carboxamide(A.3.27),3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-indan-4-yl)-1-methyl-pyrazole-4-carboxamide(A.3.28),N-[2-[2-chloro-4-(trifluoromethyl)phenoxy]phenyl]-3-(difluoromethyl)-5-fluoro-1-methyl-pyrazole-4-carboxamide(A.3.29), methyl(E)-2-[2-[(5-cyano-2-methyl-phenoxy)methyl]phenyl]-3-methoxy-prop-2-enoate(A.3.30),N-[(5-chloro-2-isopropyl-phenyl)methyl]-N-cyclopropyl-3-(difluoromethyl)-5fluoro-1-methyl-pyrazole-4-carboxamide (A.3.31),2-(difluoromethyl)-N-(1,1,3-trimethyl-indan-4-yl)pyridine-3-carboxamide(A.3.32),2-(difluoromethyl)-N-[(3R)-1,1,3-trimethylindan-4-yl]pyridine-3-carboxamide(A.3.33),2-(difluoromethyl)-N-(3-ethyl-1,1-dimethyl-indan-4-yl)pyridine-3-carboxamide(A.3.34),2-(difluoromethyl)-N-[(3R)-3-ethyl-1,1-dimethyl-indan-4-yl]pyridine-3-carboxamide(A.3.35),2-(difluoromethyl)-N-(1,1-dimethyl-3-propyl-indan-4-yl)pyridine-3-carboxamide(A.3.36),2-(difluoromethyl)-N-[(3R)-1,1-dimethyl-3-propyl-indan-4-yl]pyridine-3-carboxamide(A.3.37),2-(difluoromethyl)-N-(3-isobutyl-1,1-dimethyl-indan-4-yl)pyridine-3-carboxamide(A.3.38), 2-(difluoromethyl)-N-[(3R)-3-isobutyl-1,1-dimethyl-indan-4yl]pyridine-3-carboxamide (A.3.39); Other respiration inhibitors:diflumetorim (A.4.1); nitrophenyl derivates: binapacryl (A.4.2),dinobuton (A.4.3), dinocap (A.4.4), fluazinam (A.4.5), meptyldinocap(A.4.6), ferimzone (A.4.7); organometal compounds: fentin salts, e. g.fentin-acetate (A.4.8), fentin chloride (A.4.9) or fentin hydroxide(A.4.10); ametoctradin (A.4.11); silthiofam (A.4.12); B) Sterolbiosynthesis inhibitors (SBI fungicides) C14 demethylase inhibitors:triazoles: azaconazole (B.1.1), bitertanol (B.1.2), bromuconazole(B.1.3), cyproconazole (B.1.4), difenoconazole (B.1.5), diniconazole(B.1.6), diniconazole-M (B.1.7), epoxiconazole (B.1.8), fenbuconazole(B.1.9), fluquinconazole (B.1.10), flusilazole (B.1.11), flutriafol(B.1.12), hexaconazole (B.1.13), imibenconazole (B.1.14), ipconazole(B.1.15), metconazole (B.1.17), myclobutanil (B.1.18), oxpoconazole(B.1.19), paclobutrazole (B.1.20), penconazole (B.1.21), propiconazole(B.1.22), prothioconazole (B.1.23), simeconazole (B.1.24), tebuconazole(B.1.25), tetraconazole (B.1.26), triadimefon (B.1.27), triadimenol(B.1.28), triticonazole (B.1.29), uniconazole (B.1.30),1-[rel-(2S;3R)-3-(2-chloro-phenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-5-thiocyanato-1H-[1,2,4]triazole(B.1.31),2-[rel-(2S;3R)-3-(2-chlorophenyl)-2-(2,4-difluorophenyl)-oxiranylmethyl]-2H-[1,2,4]triazole-3-thiol(B.1.32),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)pentan-2-ol(B.1.33),1-[4-(4-chlorophenoxy)-2-(trifluoro-methyl)phenyl]-1-cyclopropyl-2-(1,2,4-triazol-1-yl)ethanol(B.1.34),2-[4-(4-chloro-phenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.35),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.36), ipfentrifluconazole (B.1.37), mefentrifluconazole (B.1.38),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-3-methyl-1-(1,2,4-triazol-1-yl)butan-2-ol(B.1.39),2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)pentan-2-ol(B.1.40),2-[4-(4-fluorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1,2,4-triazol-1-yl)propan-2-ol(B.1.41),2-[2-chloro-4-(4-chlorophenoxy)phenyl]-1-(1,2,4-triazol-1-yl)pent-3-yn-2-ol(B.1.42),2-(chloromethyl)-2-methyl-5-(p-tolylmethyl)-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol(B.1.43); imidazoles: imazalil (B.1.44), pefurazoate (B.1.45),prochloraz (B.1.46), triflumizol (B.1.47); pyrimidines, pyridines andpiperazines: fenarimol (B.1.49), pyrifenox (B.1.50), triforine (B.1.51),[3-(4-chloro-2-fluoro-phenyl)-5-(2,4-difluorophenyl)isoxazol-4-yl]-(3-pyridyl)methanol(B.1.52); Delta14-reductase inhibitors: aldimorph (B.2.1), dodemorph(B.2.2), dodemorph-acetate (B.2.3), fenpropimorph (B.2.4), tridemorph(B.2.5), fenpropidin (B.2.6), piperalin (B.2.7), spiroxamine (B.2.8);Inhibitors of 3-keto reductase: fenhexamid (B.3.1); Other Sterolbiosynthesis inhibitors: chlorphenomizole (B.4.1); C) Nucleic acidsynthesis inhibitors Phenylamides or acyl amino acid fungicides:benalaxyl (C.1.1), benalaxyl-M (C.1.2), kiralaxyl (C.1.3), metalaxyl(C.1.4), metalaxyl-M (C.1.5), ofurace (C.1.6), oxadixyl (C.1.7); Othernucleic acid synthesis inhibitors: hymexazole (C.2.1), octhilinone(C.2.2), oxolinic acid (C.2.3), bupirimate (C.2.4), 5-fluorocytosine(C.2.5), 5-fluoro-2-(p-tolylmethoxy)pyrimidin-4-amine (C.2.6),5-fluoro-2-(4-fluorophenylmethoxy)pyrimidin-4-amine (C.2.7),5-fluoro-2-(4-chlorophenylmethoxy)pyrimidin-4 amine (C.2.8); D)Inhibitors of cell division and cytoskeleton Tubulin inhibitors: benomyl(D.1.1), carbendazim (D.1.2), fuberidazole (D1.3), thiabendazole(D.1.4), thiophanate-methyl (D.1.5),3-chloro-4-(2,6-difluorophenyl)-6-methyl-5-phenyl-pyridazine (D.1.6),3-chloro-6-methyl-5-phenyl-4-(2,4,6-trifluorophenyl)pyridazine (D.1.7),N-ethyl-2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]butanamide (D.1.8),N-ethyl-2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methylsulfanyl-acetamide(D.1.9),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-fluoroethyl)butanamide(D.1.10),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-flu-oroethyl)-2-methoxy-acetamide(D.1.11), 2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-propyl-butanamide(D.1.12),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methoxy-N-propyl-acetamide(D.1.13),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-2-methylsulfanyl-N-propyl-acetamide(D.1.14),2-[(3-ethynyl-8-methyl-6-quinolyl)oxy]-N-(2-fluoroethyl)-2-methylsulfanyl-acetamide(D.1.15),4-(2-bromo-4-fluoro-phenyl)-N-(2-chloro-6-fluoro-phenyl)-2,5-dimethyl-pyrazol-3-amine(D.1.16); Other cell division inhibitors: diethofencarb (D.2.1),ethaboxam (D.2.2), pencycuron (D.2.3), fluopicolide (D.2.4), zoxamide(D.2.5), metrafenone (D.2.6), pyriofenone (D.2.7). E) Inhibitors ofamino acid and protein synthesis Methionine synthesis inhibitors:cyprodinil (E.1.1), mepanipyrim (E.1.2), pyrimethanil (E.1.3); Proteinsynthesis inhibitors: blasticidin-S(E.2.1), kasugamycin (E.2.2),kasugamycin hydrochloride-hydrate (E.2.3), mildiomycin (E.2.4),streptomycin (E.2.5), oxytetracyclin (E.2.6); F) Signal transductioninhibitors MAP/histidine kinase inhibitors: fluoroimid (F.1.1),iprodione (F.1.2), procymidone (F.1.3), vinclozolin (F.1.4), fludioxonil(F.1.5); G protein inhibitors: quinoxyfen (F.2.1); G) Lipid and membranesynthesis inhibitors Phospholipid biosynthesis inhibitors: edifenphos(G.1.1), iprobenfos (G.1.2), pyrazophos (G.1.3), isoprothiolane (G.1.4);Lipid peroxidation: dicloran (G.2.1), quintozene (G.2.2), tecnazene(G.2.3), tolclofos-methyl (G.2.4), biphenyl (G.2.5), chloroneb (G.2.6),etridiazole (G.2.7); Phospholipid biosynthesis and cell wall deposition:dimethomorph (G.3.1), flumorph (G.3.2), mandipropamid (G.3.3), pyrimorph(G.3.4), benthiavalicarb (G.3.5), iprovalicarb (G.3.6), valifenalate(G.3.7); Compounds affecting cell membrane permeability and fattyacides: propamocarb (G.4.1); Inhibitors of oxysterol binding protein:oxathiapiprolin (G.5.1),2-{3-[2-(1-{[3,5-bis(difluoromethyl-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenylmethanesulfonate (G.5.2),2-{3-[2-(1-{[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorophenylmethanesulfonate (G.5.3),4-[1-[2-[3-(difluoromethyl)-5-methyl-pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.4),4-[1-[2-[3,5-bis(difluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.5),4-[1-[2-[3-(difluoromethyl)-5-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.6),4-[1-[2-[5-cyclopropyl-3-(difluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.7),4-[1-[2-[5-methyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.8),4-[1-[2-[5-(difluoromethyl)-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.9),4-[1-[2-[3,5-bis(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.10),(4-[1-[2-[5-cyclopropyl-3-(trifluoromethyl)pyrazol-1-yl]acetyl]-4-piperidyl]-N-tetralin-1-yl-pyridine-2-carboxamide(G.5.11); H) Inhibitors with Multi Site Action Inorganic activesubstances: Bordeaux mixture (H.1.1), copper (H.1.2), copper acetate(H.1.3), copper hydroxide (H.1.4), copper oxychloride (H.1.5), basiccopper sulfate (H.1.6), sulfur (H.1.7); Thio- and dithiocarbamates:ferbam (H.2.1), mancozeb (H.2.2), maneb (H.2.3), metam (H.2.4), metiram(H.2.5), propineb (H.2.6), thiram (H.2.7), zineb (H.2.8), ziram (H.2.9);Organochlorine compounds: anilazine (H.3.1), chlorothalonil (H.3.2),captafol (H.3.3), captan (H.3.4), folpet (H.3.5), dichlofluanid (H.3.6),dichlorophen (H.3.7), hexachlorobenzene (H.3.8), pentachlorphenole(H.3.9) and its salts, phthalide (H.3.10), tolylfluanid (H.3.11);Guanidines and others: guanidine (H.4.1), dodine (H.4.2), dodine freebase (H.4.3), guazatine (H.4.4), guazatine-acetate (H.4.5), iminoctadine(H.4.6), iminoctadine-triacetate (H.4.7), iminoctadine-tris(albesilate)(H.4.8), dithianon (H.4.9),2,6-di-methyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c′]dipyrrole-1,3,5,7(2H,6H)-tetraone(H.4.10); I) Cell wall synthesis inhibitors Inhibitors of glucansynthesis: validamycin (I.1.1), polyoxin B (I.1.2); Melanin synthesisinhibitors: pyroquilon (I.2.1), tricyclazole (I.2.2), carpropamid(I.2.3), dicyclomet (I.2.4), fenoxanil (I.2.5); J) Plant defenceinducers Acibenzolar-S-methyl (J.1.1), probenazole (J.1.2), isotianil(J.1.3), tiadinil (J.1.4), prohexadione-calcium (J.1.5); phosphonates:fosetyl (J.1.6), fosetyl-aluminum (J.1.7), phosphorous acid and itssalts (J.1.8), potassium or sodium bicarbonate (J.1.9),4-cyclopropyl-N-(2,4-dimethoxyphenyl)thiadiazole-5-carboxamide (J.1.10),calcium phosphonate (J.1.11), potassium phosphonate (J.1.12); K) Unknownmode of action Bronopol (K.1.1), chinomethionat (K.1.2), cyflufenamid(K.1.3), cymoxanil (K.1.4), dazomet (K.1.5), debacarb (K.1.6),diclocymet (K.1.7), diclomezine (K.1.8), difenzoquat (K.1.9),difenzoquat-methylsulfate (K.1.10), diphenylamin (K.1.11), fenitropan(K.1.12), fenpyrazamine (K.1.13), flumetover (K.1.14), flusulfamide(K.1.15), flutianil (K.1.16), harpin (K.1.17), methasulfocarb (K.1.18),nitrapyrin (K.1.19), nitrothal-isopropyl (K.1.20), tolprocarb (K.1.21),oxin-copper (K.1.22), proquinazid (K.1.23), tebufloquin (K.1.24),tecloftalam (K.1.25), triazoxide (K.1.26),N′-(4-(4-chloro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methylformamidine (K.1.27),N′-(4-(4-fluoro-3-trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methylformamidine (K.1.28),N′-[4-[[3-[(4-chlorophenyl)methyl]-1,2,4-thiadiazol-5-yl]oxy]-2,5-dimethyl-phenyl]-N-ethyl-N-methyl-formamidine(K.1.29),N′-(5-bromo-6-indan-2-yloxy-2-methyl-3-pyridyl)-N-ethyl-N-methyl-formamidine(K.1.30),N′-[5-bromo-6-[1-(3,5-difluorophenyl)ethoxy]-2-methyl-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.31),N′-[5-bromo-6-(4-isopropylcyclohexoxy)-2-methyl-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.32),N′-[5-bromo-2-methyl-6-(1-phenylethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.33),N′-(2-methyl-5-trifluoromethyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methylformamidine (K.1.34),N′-(5-difluoromethyl-2-methyl-4-(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methylformamidine (K.1.35),2-(4-chloro-phenyl)-N-[4-(3,4-dimethoxy-phenyl)-isoxazol-5-yl]-2-prop-2-ynyloxy-acetamide(K.1.36),3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine(pyrisoxazole) (K.1.37),3-[5-(4-methylphenyl)-2,3-dimethyl-isoxazolidin-3 yl]-pyridine (K.1.38),5-chloro-1-(4,6-dimethoxy-pyrimidin-2-yl)-2-methyl-1H-benzoimidazole(K.1.39), ethyl (Z)-3-amino-2-cyano-3-phenyl-prop-2-enoate (K.1.40),picarbutrazox (K.1.41), pentylN-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carbamate(K.1.42), but-3-ynylN-[6-[[(Z)-[(1-methyltetrazol-5-yl)-phenyl-methylene]amino]oxymethyl]-2-pyridyl]carbamate(K.1.43),2-[2-[(7,8-difluoro-2-methyl-3-quinolyl)oxy]-6-fluoro-phenyl]propan-2-ol(K.1.44),2-[2-fluoro-6-[(8-fluoro-2-methyl-3-quinolyl)oxy]phen-yl]propan-2-ol(K.1.45),3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-1-yl)quinoline(K.1.46), quinofumelin (K.1.47),3-(4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinoline(K.1.48), 9-fluoro-2,2-dimethyl-5-(3-quinolyl)-3H-1,4-benzoxazepine(K.1.49), 2-(6-benzyl-2-pyridyl)quinazoline (K.1.50),2-[6-(3-fluoro-4-methoxy-phenyl)-5-methyl-2-pyridyl]quinazoline(K.1.51), dichlobentiazox (K.1.52),N′-(2,5-dimethyl-4-phenoxy-phenyl)-N-ethyl-N-methyl-formamidine(K.1.53),N′-[5-bromo-2-methyl-6-(1-methyl-2-propoxy-ethoxy)-3-pyridyl]-N-ethyl-N-methyl-formamidine(K.1.54); M) Growth regulators abscisic acid (M.1.1), amidochlor,ancymidol, 6-benzylaminopurine, brassinolide, butralin, chlormequat,chlormequat chloride, choline chloride, cyclanilide, daminozide,dikegulac, dimethipin, 2,6-dimethylpuridine, ethephon, flumetralin,flurprimidol, fluthiacet, forchlorfenuron, gibberellic acid, inabenfide,indole-3-acetic acid, maleic hydrazide, mefluidide, mepiquat, mepiquatchloride, naphthaleneacetic acid, N-6-benzyladenine, paclobutrazol,prohexadione, prohexadione-calcium, prohydrojasmon, thidiazuron,triapenthenol, tributyl phosphorotrithioate, 2,3,5-tri-iodobenzoic acid,trinexapac-ethyl and uniconazole; N) Herbicides from classes N.1 to N.15N.1 Lipid biosynthesis inhibitors: alloxydim (N.1.1), alloxydim-sodium(N.1.2), butroxydim (N.1.3), clethodim (N.1.4), clodinafop (N.1.5),clodinafop-propargyl (N.1.6), cycloxydim (N.1.7), cyhalofop (N.1.8),cyhalofop-butyl (N.1.9), diclofop(N.1.10), diclofop-methyl (N.1.11),fenoxaprop (N.1.12), fenoxaprop-ethyl (N.1.13), fenoxaprop-P (N.1.14),fenoxaprop-P-ethyl (N.1.15), fluazifop (N.1.16), fluazifop-butyl(N.1.17), fluazifop-P (N.1.18), fluazifop-P-butyl (N.1.19), haloxyfop(N.1.20), haloxyfop-methyl (N.1.21), haloxyfop-P (N.1.22),haloxyfop-P-methyl (N.1.23), metamifop (N.1.24), pinoxaden (N.1.25),profoxydim (N.1.26), propaquizafop (N.1.27), quizalofop (N.1.28),quizalofop-ethyl (N.1.29), quizalofop-tefuryl (N.1.30), quizalofop-P(N.1.31), quizalofop-P-ethyl (N.1.32), quizalofop-P-tefuryl (N.1.33),sethoxydim (N.1.34), tepraloxydim (N.1.35), tralkoxydim (N.1.36),4-(4′-chloro-4-cyclo¬propyl-2′-fluoro[1,1′-biphenyl]-3-y)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.37) CAS 1312337-72-6);4-(2′,4′-dichloro-4-cyclopropyl[1,1′-biphenyl]-3-yl)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.38) CAS 1312337-45-3);4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-y)-5-hydroxy-2,2,6,6-tetramethyl-2H-pyran-3(6H)-one((N.1.39) CAS 1033757-93-5);4-(2′,4′-Dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-2,2,6,6-tetramethyl-2H-pyran-3,5(4H,6H)-dione((N.1.40) CAS 1312340-84-3);5-(acetyloxy)-4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.41) CAS 1312337-48-6);5-(acetyloxy)-4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one(N.1.42);5-(acetyloxy)-4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.43) CAS 1312340-82-1);5-(acetyloxy)-4-(2′,4′-dichloro-4-ethyl[1,1′-biphenyl]-3-yl)-3,6-dihydro-2,2,6,6-tetramethyl-2H-pyran-3-one((N.1.44) CAS 1033760-55-2);4-(4′-chloro-4-cyclopropyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.45) CAS 1312337-51-1);4-(2′,4′-dichloro-4-cyclopropyl-[1,1′-biphenyl]-3-y)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester (N.1.46);4-(4′-chloro-4-ethyl-2′-fluoro[1,1′-biphenyl]-3-yl)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.47) CAS 1312340-83-2);4-(2′,4′-dichloro-4-ethyl,[1,1′-biphenyl]-3-y)-5,6-dihydro-2,2,6,6-tetramethyl-5-oxo-2H-pyran-3-ylcarbonic acid methyl ester ((N.1.48) CAS 1033760-58-5); benfuresate(N.1.49), butylate (N.1.50), cycloate (N.1.51), dalapon (N.1.52),dimepiperate (N.1.53), EPTC (N.1.54), esprocarb (N.1.55), ethofumesate(N.1.56), flupropanate (N.1.57), molinate (N.1.58), orbencarb (N.1.59),pebulate (N.1.60), prosulfocarb (N.1.61), TCA (N.1.62), thiobencarb(N.1.63), tiocarbazil (N.1.64), triallate (N.1.65) and vernolate(N.1.66); N.2 ALS inhibitors: amidosulfuron (N.2.1), azimsulfuron(N.2.2), bensulfuron (N.2.3), bensulfuron-methyl (N.2.4), chlorimuron(N.2.5), chlorimuron-ethyl (N.2.6), chlorsulfuron (N.2.7), cinosulfuron(N.2.8), cyclosulfamuron (N.2.9), ethametsulfuron (N.2.10),ethametsulfuron-methyl (N.2.11), ethoxysulfuron (N.2.12), flazasulfuron(N.2.13), flucetosulfuron (N.2.14), flupyrsulfuron (N.2.15),flupyrsulfuron-methyl-sodium (N.2.16), foramsulfuron (N.2.17),halosulfuron (N.2.18), halosulfuron-methyl (N.2.19), imazosulfuron(N.2.20), iodosulfuron (N.2.21), iodosulfuron-methyl-sodium (N.2.22),iofensulfuron (N.2.23), iofensulfuron-sodium (N.2.24), mesosulfuron(N.2.25), metazosulfuron (N.2.26), metsulfuron (N.2.27),metsulfuron-methyl (N.2.28), nicosulfuron (N.2.29), orthosulfamuron(N.2.30), oxasulfuron (N.2.31), primisulfuron (N.2.32),primisulfuron-methyl (N.2.33), propyrisulfuron (N.2.34), prosulfuron(N.2.35), pyrazosulfuron (N.2.36), pyrazosulfuron-ethyl (N.2.37),rimsulfuron (N.2.38), sulfometuron (N.2.39), sulfometuron-methyl(N.2.40), sulfosulfuron (N.2.41), thifensulfuron (N.2.42),thifensulfuron-methyl (N.2.43), triasulfuron (N.2.44), tribenuron(N.2.45), tribenuron-methyl (N.2.46), trifloxysulfuron (N.2.47),triflusulfuron (N.2.48), triflusulfuron-methyl (N.2.49), tritosulfuron(N.2.50), imazamethabenz (N.2.51), imazamethabenz-methyl (N.2.52),imazamox (N.2.53), imazapic (N.2.54), imazapyr (N.2.55), imazaquin(N.2.56), imazethapyr (N.2.57); cloransulam (N.2.58), cloransulam-methyl(N.2.59), diclosulam (N.2.60), flumetsulam (N.2.61), florasulam(N.2.62), metosulam (N.2.63), penoxsulam (N.2.64), pyrimisulfan (N.2.65)and pyroxsulam (N.2.66); bispyribac (N.2.67), bispyribac-sodium(N.2.68), pyribenzoxim (N.2.69), pyriftalid (N.2.70), pyriminobac(N.2.71), pyriminobac-methyl (N.2.72), pyrithiobac (N.2.73),pyrithiobac-sodium (N.2.74),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]methyl]amino]-benzoicacid-1-methyl¬ethyl ester ((N.2.75) CAS 420138-41-6),4-[[[2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]phenyl]¬methyl]amino]-benzoicacid propyl ester ((N.2.76) CAS 420138-40-5),N-(4-bromophenyl)-2-[(4,6-dimethoxy-2-pyrimidinyl)oxy]-benzenemethanamine((N.2.77) CAS 420138-01-8); flucarbazone (N.2.78), flucarbazone-sodium(N.2.79), propoxycarbazone (N.2.80), propoxycarbazone-sodium (N.2.81),thiencarbazone (N.2.82), thiencarbazone-methyl (N.2.83), triafamone(N.2.84); N.3 Photosynthesis inhibitors: amicarbazone (N.3.1);chlorotriazine (N.3.2); ametryn (N.3.3), atrazine (N.3.4), chloridazone(N.3.5), cyanazine (N.3.6), desmetryn (N.3.7), dimethametryn(N.3.8),hexazinone (N.3.9), metribuzin (N.3.10), prometon (N.3.11),prometryn (N.3.12), propazine (N.3.13), simazine (N.3.14), simetryn(N.3.15), terbumeton (N.3.16), terbuthylazin (N.3.17), terbutryn(N.3.18), trietazin (N.3.19); chlorobromuron (N.3.20), chlorotoluron(N.3.21), chloroxuron (N.3.22), dimefuron (N.3.23), diuron (N.3.24),fluometuron (N.3.25), isoproturon (N.3.26), isouron (N.3.27), linuron(N.3.28), metamitron (N.3.29), methabenzthiazuron (N.3.30), metobenzuron(N.3.31), metoxuron (N.3.32), monolinuron (N.3.33), neburon (N.3.34),siduron (N.3.35), tebuthiuron (N.3.36), thiadiazuron (N.3.37),desmedipham (N.3.38), karbutilat (N.3.39), phenmedipham (N.3.40),phenmedipham-ethyl (N.3.41), bromofenoxim (N.3.42), bromoxynil (N.3.43)and its salts and esters, ioxynil (N.3.44) and its salts and esters,bromacil (N.3.45), lenacil (N.3.46), terbacil (N.3.47), bentazon(N.3.48), bentazon-sodium (N.3.49), pyridate (N.3.50), pyridafol(N.3.51), pentanochlor (N.3.52), propanil (N.3.53); diquat (N.3.54),diquat-dibromide (N.3.55), paraquat (N.3.56), paraquat-dichloride(N.3.57), paraquat-dimetilsulfate (N.3.58); N.4 protoporphyrinogen-IXoxidase inhibitors: acifluorfen (N.4.1), acifluorfen-sodium (N.4.2),azafenidin (N.4.3), bencarbazone (N.4.4), benzfendizone (N.4.5), bifenox(N.4.6), butafenacil (N.4.7), carfentrazone (N.4.8), carfentrazone-ethyl(N.4.9), chlormethoxyfen (N.4.10), cinidon-ethyl (N.4.11), fluazolate(N.4.12), flufenpyr (N.4.13), flufenpyr-ethyl (N.4.14), flumiclorac(N.4.15), flumiclorac-pentyl (N.4.16), flumioxazin (N.4.17),fluoroglycofen (N.4.18), fluoroglycofen-ethyl (N.4.19), fluthiacet(N.4.20), fluthiacet-methyl (N.4.21), fomesafen (N.4.22), halosafen(N.4.23), lactofen (N.4.24), oxadiargyl (N.4.25), oxadiazon (N.4.26),oxyfluorfen (N.4.27), pentoxazone (N.4.28), profluazol (N.4.29),pyraclonil (N.4.30), pyraflufen (N.4.31), pyraflufen-ethyl (N.4.32),saflufenacil (N.4.33), sulfentrazone (N.4.34), thidiazimin (N.4.35),tiafenacil (N.4.36), trifludimoxazin (N.4.37), ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate((N.4.38) CAS 353292-31-6),N-ethyl-3-(2,6-dichloro-4-trifluoro-methylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.39) CAS 452098-92-9), Ntetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.40) CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethyl¬phenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.41) CAS 452099-05-7), Ntetrahydro¬furfuryl-3-(2-chloro-6-fluoro-4-trifluoro-methylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide((N.4.42) CAS 452100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione((N.4.43) CAS 451484-50-7),2-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dione((N.4.44) CAS 1300118-96-0),1-methyl-6-trifluoro¬methyl-3-(2,2,7-tri-fluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione((N.4.45) CAS 1304113-05-0), methyl(E)-4-[2-chloro-5-[4-chloro-5-(difluoromethoxy)-1H-methyl-pyrazol-3-yl]-4-fluoro-phenoxy]-3-methoxy-but-2-enoate((N.4.46) CAS 948893-00-3),3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)-1H-pyrimidine-2,4-dione((N.4.47) CAS 212754-02-4); N.5 Bleacher herbicides: beflubutamid(N.5.1), diflufenican (N.5.2), fluridone (N.5.3), flurochloridone(N.5.4), flurtamone (N.5.5), norflurazon (N.5.6), picolinafen (N.5.7),4-(3-trifluoromethyl¬phenoxy)-2-(4-trifluoromethylphenyl),pyrimidine((N.5.8) CAS 180608-33-7); benzobicyclon (N.5.9), benzofenap (N.5.10),bicyclopyrone (N.5.11), clomazone (N.5.12), fenquintrione (N.5.13),isoxaflutole (N.5.14), mesotrione (N.5.15), pyrasulfotole (N.5.16),pyrazolynate (N.5.17), pyrazoxyfen (N.5.18), sulcotrione (N.5.19),tefuryltrione (N.5.20), tembotrione (N.5.21), tolpyralate (N.5.22),topramezone (N.5.23); aclonifen (N.5.24), amitrole (N.5.25), flumeturon(N.5.26); N.6 EPSP synthase inhibitors: glyphosate (N.6.1),glyphosate-isopropylammonium (N.6.2), glyposate-potassium (N.6.3),glyphosate-trimesium (sulfosate) (N.6.4); N.7 Glutamine synthaseinhibitors: bilanaphos (bialaphos) (N.7.1), bilanaphos-sodium (N.7.2),glufosinate (N.7.3), glufosinate-P (N.7.4), glufosinate-ammonium(N.7.5); N.8 DHP synthase inhibitors: asulam (N.8.1); N.9 Mitosisinhibitors: benfluralin (N.9.1), butralin (N.9.2), dinitramine (N.9.3),ethalfluralin (N.9.4), fluchloralin (N.9.5), oryzalin (N.9.6),pendimethalin (N.9.7), prodiamine (N.9.8), trifluralin (N.9.9);amiprophos (N.9.10), amiprophos-methyl (N.9.11), butamiphos (N.9.12);chlorthal (N.9.13), chlorthal-dimethyl (N.9.14), dithiopyr (N.9.15),thiazopyr (N.9.16), propyzamide (N.9.17), tebutam (N.9.18); carbetamide(N.9.19), chlorpropham (N.9.20), flamprop (N.9.21), flamprop-isopropyl(N.9.22), flamprop-methyl (N.9.23), flamprop-M-isopropyl (N.9.24),flamprop-M-methyl (N.9.25), propham (N.9.26); N.10 VLCFA inhibitors:acetochlor (N.10.1), alachlor (N.10.2), butachlor (N.10.3), dimethachlor(N.10.4), dimethenamid (N.10.5), dimethenamid-P (N.10.6), metazachlor(N.10.7), metolachlor (N.10.8), metolachlor-S(N.10.9), pethoxamid(N.10.10), pretilachlor (N.10.11), propachlor (N.10.12), propisochlor(N.10.13), thenylchlor (N.10.14), flufenacet (N.10.15), mefenacet(N.10.16), diphenamid (N.10.17), naproanilide (N.10.18), napropamide(N.10.19), napropamide-M (N.10.20), fentrazamide (N.10.21), anilofos(N.10.22), cafenstrole (N.10.23), fenoxasulfone (N.10.24),ipfencarbazone (N.10.25), piperophos (N.10.26), pyroxasulfone (N.10.27),isoxazoline compounds of the formulae II.1, II.2, II.3, II.4, II.5,II.6, II.7, II.8 and II.9

N.11 Cellulose biosynthesis inhibitors: chlorthiamid (N.11.1),dichlobenil (N.11.2), flupoxam (N.11.3), indaziflam (N.11.4), isoxaben(N.11.5), triaziflam (N.11.6),1-cyclohexyl-5-pentafluorphenyloxy-14-[1,2,4,6]thiatriazin-3-ylamine((N.11.7) CAS 175899-01-1); N.12 Decoupler herbicides: dinoseb (N.12.1),dinoterb (N.12.2), DNOC (N.12.3) and its salts; N.13 Auxinic herbicides:2,4-D (N.13.1) and its salts and esters, clacyfos (N.13.2), 2,4-DB(N.13.3) and its salts and esters, aminocyclopyrachlor (N.13.4) and itssalts and esters, aminopyralid (N.13.5) and its salts such asaminopyralid-dimethylammonium (N.13.6),aminopyralid-tris(2-hydroxypropyl)ammonium (N.13.7) and its esters,benazolin (N.13.8), benazolin-ethyl (N.13.9), chloramben (N.13.10) andits salts and esters, clomeprop (N.13.11), clopyralid (N.13.12) and itssalts and esters, dicamba (N.13.13) and its salts and esters,dichlorprop (N.13.14) and its salts and esters, dichlorprop-P (N.13.15)and its salts and esters, fluroxypyr (N.13.16), fluroxypyr-butometyl(N.13.17), fluroxypyr-meptyl (N.13.18), halauxifen (N.13.) and its saltsand esters (CAS 943832-60-8); MCPA (N.13.) and its salts and esters,MCPA-thioethyl (N.13.19), MCPB (N.13.20) and its salts and esters,mecoprop (N.13.21) and its salts and esters, mecoprop-P (N.13.22) andits salts and esters, picloram (N.13.23) and its salts and esters,quinclorac (N.13.24), quinmerac (N.13.25), TBA (2,3,6) (N.13.26) and itssalts and esters, triclopyr (N.13.27) and its salts and esters,4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylicacid (N.13.28), benzyl4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylate((N.13.29) CAS 1390661-72-9); N.14 Auxin transport inhibitors:diflufenzopyr (N.14.1), diflufenzopyr-sodium (N.14.2), naptalam (N.14.3)and naptalam-sodium (N.14.4); N.15 Other herbicides: bromobutide(N.15.1), chlorflurenol (N.15.2), chlorflurenol-methyl (N.15.3),cinmethylin (N.15.4), cumyluron (N.15.5), cyclopyrimorate ((N.15.6) CAS499223-49-3) and its salts and esters, dalapon (N.15.7), dazomet(N.15.8), difenzoquat (N.15.9), difenzoquat-metilsulfate (N.15.10),dimethipin (N.15.11), DSMA (N.15.12), dymron (N.15.13), endothal(N.15.14) and its salts, etobenzanid (N.15.15), flurenol (N.15.16),flurenol-butyl (N.15.17), flurprimidol (N.15.18), fosamine (N.15.19),fosamine-ammonium (N.15.20), indanofan (N.15.21), maleic hydrazide(N.15.22), mefluidide (N.15.23), metam (N.15.24), methiozolin ((N.15.25)CAS 403640-27-7), methyl azide (N.15.26), methyl bromide (N.15.27),methyl-dymron (N.15.28), methyl iodide (N.15.29), MSMA (N.15.30), oleicacid (N.15.31), oxaziclomefone (N.15.32), pelargonic acid (N.15.33),pyributicarb (N.15.34), quinoclamine (N.15.35), tridiphane (N.15.36); O)Insecticides from classes O.1 to O.29 O.1 Acetylcholine esterase (AChE)inhibitors: aldicarb (O.1.1), alanycarb (O.1.2), bendiocarb (O.1.3),benfuracarb (O.1.4), butocarboxim (O.1.5), butoxycarboxim (O.1.6),carbaryl (O.1.7), carbofuran (O.1.8), carbosulfan (O.1.9), ethiofencarb(O.1.10), fenobucarb (O.1.11), formetanate (O.1.12), furathiocarb(O.1.13), isoprocarb (O.1.14), methiocarb (O.1.15), methomyl (O.1.16),metolcarb (O.1.17), oxamyl (O.1.18), pirimicarb (O.1.19), propoxur(O.1.20), thiodicarb (O.1.21), thiofanox (O.1.22), trimethacarb(O.1.23), XMC (O.1.24), xylylcarb (O.1.25) and triazamate (O.1.26);acephate (O.1.27), azamethiphos (O.1.28), azinphos-ethyl (O.1.29),azinphosmethyl (O.1.30), cadusafos (O.1.31), chlorethoxyfos (O.1.32),chlorfenvinphos (O.1.33), chlormephos (O.1.34), chlorpyrifos (O.1.35),chlorpyrifos-methyl (O.1.36), coumaphos (O.1.37), cyanophos (O.1.38),demeton-S-methyl (O.1.39), diazinon (O.1.40), dichlorvos/DDVP (O.1.41),dicrotophos (O.1.42), dimethoate (O.1.43), dimethylvinphos (O.1.44),disulfoton (O.1.45), EPN (O.1.46), ethion (O.1.47), ethoprophos(O.1.48), famphur (O.1.49), fenamiphos (O.1.50), fenitrothion (O.1.51),fenthion (O.1.52), fosthiazate (O.1.53), heptenophos (O.1.54), imicyafos(O.1.55), isofenphos (O.1.56), isopropyl O-(methoxyaminothio-phosphoryl)salicylate (O.1.57), isoxathion (O.1.58), malathion (O.1.59), mecarbam(O.1.60), methamidophos (O.1.61), methidathion (O.1.62), mevinphos(O.1.63), monocrotophos (O.1.64), naled (O.1.65), omethoate (O.1.66),oxydemeton-methyl (O.1.67), parathion (O.1.68), parathion-methyl(O.1.69), phenthoate (O.1.70), phorate (O.1.71), phosalone (O.1.72),phosmet (O.1.73), phosphamidon (O.1.74), phoxim (O.1.75),pirimiphos-methyl (O.1.76), profenofos (O.1.77), propetamphos (O.1.78),prothiofos (O.1.79), pyraclofos (O.1.80), pyridaphenthion (O.1.81),quinalphos (O.1.82), sulfotep (O.1.83), tebupirimfos (O.1.84), temephos(O.1.85), terbufos (O.1.86), tetrachlorvinphos (O.1.87), thiometon(O.1.88), triazophos (O.1.89), trichlorfon (O.1.90), vamidothion(O.1.91); O.2 GABA-gated chloride channel antagonists: endosulfan(O.2.1), chlordane (O.2.2); ethiprole (O.2.3), fipronil (O.2.4),flufiprole (O.2.5), pyrafluprole (O.2.6), pyriprole (O.2.7); O.3 Sodiumchannel modulators: acrinathrin (O.3.1), allethrin (O.3.2), d-cis-transallethrin (O.3.3), d-trans allethrin (O.3.4), bifenthrin (O.3.5),bioallethrin (O.3.6), bioallethrin S-cylclopentenyl (O.3.7),bioresmethrin (O.3.8), cycloprothrin (O.3.9), cyfluthrin (O.3.10),beta-cyfluthrin (O.3.11), cyhalothrin (O.3.12), lambda-cyhalothrin(O.3.13), gamma-cyhalothrin (O.3.14), cypermethrin (O.3.15),alpha-cypermethrin (O.3.16), beta-cypermethrin (O.3.17),theta-cypermethrin (O.3.18), zeta-cypermethrin (O.3.19), cyphenothrin(O.3.20), deltamethrin (O.3.21), empenthrin (O.3.22), esfenvalerate(O.3.23), etofenprox (O.3.24), fenpropathrin (O.3.25), fenvalerate(O.3.26), flucythrinate (O.3.27), flumethrin (O.3.28), tau-fluvalinate(O.3.29), halfenprox (O.3.30), heptafluthrin (O.3.31), imiprothrin(O.3.32), meperfluthrin (O.3.33), metofluthrin (O.3.34), momfluorothrin(O.3.35), permethrin (O.3.36), phenothrin (O.3.37), prallethrin(O.3.38), profluthrin (O.3.39), pyrethrin (pyrethrum) (O.3.40),resmethrin (O.3.41), silafluofen (O.3.42), tefluthrin (O.3.43),tetramethylfluthrin (O.3.44), tetramethrin (O.3.45), tralomethrin(O.3.46) and transfluthrin (O.3.47); DDT (O.3.48), methoxychlor(O.3.49); O.4 Nicotinic acetylcholine receptor agonists (nAChR):acetamiprid (O.4.1), clothianidin (O.4.2), cycloxaprid (O.4.3),dinotefuran (O.4.4), imidacloprid (O.4.5), nitenpyram (O.4.6),thiacloprid (O.4.7), thiamethoxam (O.4.8);(2E)-1-[(6-chloropyridin-3-yl)methyl]-N′-nitro-2-pentylidenehydrazinecarboximidamide(O.4.9);1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-5-propoxy-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridine(O.4.10); nicotine (O.4.11); O.5 Nicotinic acetylcholine receptorallosteric activators: spinosad (O.5.1), spinetoram (O.5.2); O.6Chloride channel activators: abamectin (O.6.1), emamectin benzoate(O.6.2), ivermectin (O.6.3), lepimectin (O.6.4), milbemectin (O.6.5);O.7 Juvenile hormone mimics: hydroprene (O.7.1), kinoprene (O.7.2),methoprene (O.7.3); fenoxycarb (O.7.4), pyriproxyfen (O.7.5); O.8miscellaneous non-specific (multi-site) inhibitors: methyl bromide(O.8.1) and other alkyl halides; chloropicrin (O.8.2), sulfuryl fluoride(O.8.3), borax (O.8.4), tartar emetic (O.8.5); O.9 Selective homopteranfeeding blockers: pymetrozine (O.9.1), flonicamid (O.9.2); O.10 Mitegrowth inhibitors: clofentezine (O.10.1), hexythiazox (O.10.2),diflovidazin (O.10.3); etoxazole (O.10.4); O.11 Microbial disruptors ofinsect midgut membranes: the Bt crop proteins: Cry1Ab, Cry1Ac, Cry1Fa,Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34/35Ab1; O.12 Inhibitors ofmitochondrial ATP synthase: diafenthiuron (O.12.1); azocyclotin(O.12.2), cyhexatin (O.12.3), fenbutatin oxide (O.12.4), propargite(O.12.5), tetradifon (O.12.6); O.13 Uncouplers of oxidativephosphorylation via disruption of the proton gradient: chlorfenapyr(O.13.1), DNOC (O.13.2), sulfluramid (O.13.3); O.14 Nicotinicacetylcholine receptor (nAChR) channel blockers: bensultap (O.14.1),cartap hydrochloride (O.14.2), thiocyclam (O.14.3), thiosultap sodium(O.14.4); O.15 Inhibitors of the chitin biosynthesis type 0:bistrifluron (O.15.1), chlorfluazuron (O.15.2), diflubenzuron (O.15.3),flucycloxuron (O.15.4), flufenoxuron (O.15.5), hexaflumuron (O.15.6),lufenuron (O.15.7), novaluron (O.15.8), noviflumuron (O.15.9),teflubenzuron (O.15.10), triflumuron (O.15.11); O.16 Inhibitors of thechitin biosynthesis type 1: buprofezin (O.16.1); O.17 Moultingdisruptors: cyromazine (O.17.1); O.18 Ecdyson receptor agonists:methoxyfenozide (O.18.1), tebufenozide (O.18.2), halofenozide (O.18.3),fufenozide (O.18.4), chromafenozide (O.18.5); O.19 Octopamin receptoragonists: amitraz (O.19.1); O.20 Mitochondrial complex III electrontransport inhibitors: hydramethylnon (O.20.1), acequinocyl (O.20.2),fluacrypyrim (O.20.3); O.21 Mitochondrial complex I electron transportinhibitors: fenazaquin (O.21.1), fenpyroximate (O.21.2), pyrimidifen(O.21.3), pyridaben (O.21.4), tebufenpyrad (O.21.5), tolfenpyrad(O.21.6); rotenone (O.21.7); O.22 Voltage-dependent sodium channelblockers: indoxacarb (O.22.1), metaflumizone (O.22.2),2-[2-(4-cyanophenyl)-1-[3-(trifluoromethyl)phenyl]-ethylidene]-N-[4-(difluoromethoxy)phenyl]-hydrazinecarboxamide(O.22.3),N-(3-chloro-2-methylphenyl)-2-[(4-chlorophenyl)-[4-[methyl(methylsulfonyl)-amino]phenyl]methylene]-hydrazinecarboxamide(O.22.4); O.23 Inhibitors of the of acetyl CoA carboxylase:spirodiclofen (O.23.1), spiromesifen (O.23.2), spirotetramat (O.23.3);O.24 Mitochondrial complex IV electron transport inhibitors: aluminiumphosphide (O.24.1), calcium phosphide (O.24.2), phosphine (O.24.3), zincphosphide (O.24.4), cyanide (O.24.5); O.25 Mitochondrial complex IIelectron transport inhibitors: cyenopyrafen (O.25.1), cyflumetofen(O.25.2); O.26 Ryanodine receptor-modulators: flubendiamide (O.26.1),chlorantraniliprole (O.26.2), cyantraniliprole (O.26.3), cyclaniliprole(O.26.4), tetraniliprole (O.26.5);(R)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide(O.26.6),(S)-3-chloro-N1-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-N2-(1-methyl-2-methylsulfonylethyl)phthalamide(O.26.7),methyl-2-[3,5-dibromo-2-({[3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazol-5-yl]carbonyl}amino)benzoyl]-1,2-dimethylhydrazinecarboxylate(O.26.8);N-[4,6-dichloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.9);N-[4-chloro-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.10);N-[4-chloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-6-methyl-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.11);N-[4,6-dichloro-2-[(di-2-propyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.12);N-[4,6-di-bromo-2-[(diethyl-lambda-4-sulfanylidene)carbamoyl]-phenyl]-2-(3-chloro-2-pyridyl)-5-(trifluoromethyl)pyrazole-3-carboxamide(O.26.13);N-[2-(5-amino-1,3,4-thiadiazol-2-yl)-4-chloro-6-methylphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide(O.26.14);3-chloro-1-(3-chloro-2-pyridinyl)-N-[2,4-dichloro-6-[[(1-cyano-1-methylethyl)amino]carbonyl]phenyl]-1H-pyrazole-5-carboxamide(O.26.15);3-bromo-N-[2,4-dichloro-6-(methylcarbamoyl)phenyl]-1-(3,5-dichloro-2-pyridyl)-1H-pyrazole-5-carboxamide(O.26.16);N-[4-chloro-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-methylphenyl]-1-(3-chloro-2-pyridinyl)-3-(fluoromethoxy)-1H-pyrazole-5-carboxamide(O.26.17); cyhalodiamide (O.26.18); O.27 insecticidal active compoundsof unknown or uncertain mode of action: afidopyropen (O.27.1),afoxolaner (O.27.2), azadirachtin (O.27.3), amidoflumet (O.27.4),benzoximate (O.27.5), bifenazate (O.27.6), broflanilide (O.27.7),bromopropylate (O.27.8), chinomethionat (O.27.9), cryolite (O.27.10),dicloromezotiaz (O.27.11), dicofol (O.27.12), flufenerim (O.27.13),flometoquin (O.27.14), fluensulfone (O.27.15), fluhexafon (O.27.16),fluopyram (O.27.17), flupyradifurone (O.27.18), fluralaner (O.27.19),metoxadiazone (O.27.20), piperonyl butoxide (O.27.21), pyflubumide(O.27.22), pyridalyl (O.27.23), pyrifluquinazon (O.27.24), sulfoxaflor(O.27.25), tioxazafen (O.27.26), triflumezopyrim (O.27.27),11-(4-chloro-2,6-dimethylphenyl)-12-hydroxy-1,4-dioxa-9-azadispiro[4.2.4.2]-tetradec-11-en-10-one(O.27.28),3-(4′-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-1-azaspiro[4.5]dec-3-en-2-one(O.27.28),1-[2-fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl]-3-(trifluoromethyl)-1H-1,2,4-triazole-5-amine(O.27.29),(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.31);(E/Z)—N-[1-[(6-chloro-5-fluoro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.32);(E/Z)-2,2,2-trifluoro-N-[1-[(6-fluoro-3-pyridyl)methyl]-2-pyridylidene]acetamide(O.27.33);(E/Z)—N-[1-[(6-bromo-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.34);(E/Z)—N-[1-[1-(6-chloro-3-pyridyl)ethyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.35);(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide(O.27.36);(E/Z)-2-chloro-N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2-difluoro-acetamide(O.27.37);(E/Z)—N-[1-[(2-chloropyrimidin-5-yl)methyl]-2-pyridylidene]-2,2,2-trifluoro-acetamide(O.27.38);(E/Z)—N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,3,3,3-pentafluoro-propanamide(O.27.39);N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-thioacetamide(O.27.40);N-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-2,2,2-trifluoro-N′-isopropyl-acetamidine(O.27.41); fluazaindolizine (O.27.42);4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]-2-methyl-N-(1-oxothietan-3-yl)benzamide(O.27.43); fluxametamide (O.27.44);5-[3-[2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy]propoxy]-1H-pyrazole(O.27.45);3-(benzoylmethylamino)-N-[2-bromo-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]-6-(trifluoromethyl)phenyl]-2-fluoro-benzamide(O.27.46);3-(benzoylmethylamino)-2-fluoro-N-[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]-benzamide(O.27.47);N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.48);N-[3-[[[2-bromo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]-2-fluorophenyl]-4-fluoro-N-methyl-benzamide(O.27.49);4-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.50);3-fluoro-N-[2-fluoro-3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-6(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-N-methyl-benzamide(O.27.51);2-chloro-N-[3-[[[2-iodo-4-[1,2,2,2-tetrafluoro-1-(tri-fluoromethyl)ethyl]-6-(trifluoromethyl)phenyl]amino]carbonyl]phenyl]-3-pyridine-carboxamide(O.27.52);4-cyano-N-[2-cyano-5-[[2,6-dibromo-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.53);4-cyano-3-[(4-cyano-2-methyl-benzoyl)amino]-N-[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]-2-fluoro-benzamide(O.27.54);N-[5-[[2-chloro-6-cyano-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.55);N-[5-[[2-bromo-6-chloro-4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.56);N-[5-[[2-bromo-6-chloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoro-methyl)propyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.57);4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,3,3,3-hexafluoro-1-(trifluoromethyl)propyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.58);4-cyano-N-[2-cyano-5-[[2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]phenyl]-2-methyl-benzamide(O.27.59);N-[5-[[2-bromo-6-chloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]carbamoyl]-2-cyano-phenyl]-4-cyano-2-methyl-benzamide(O.27.60); 2-(1,3-dioxan-2-yl)-6-[2-(3-pyridinyl)-5-thiazolyl]-pyridine;2-[6-[2-(5-fluoro-3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine(O.27.61); 2-[6-[2-(3-pyridinyl)-5-thiazolyl]-2-pyridinyl]-pyrimidine(O.27.62);N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide(O.27.63);N-methylsulfonyl-6-[2-(3-pyridyl)thiazol-5-yl]pyridine-2-carboxamide(O.27.64);N-ethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.65);N-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.66);N,2-dimethyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.67);N-ethyl-2-methyl-N-[4-methyl-2-(3-pyridyl)thiazol-5-yl]-3-methylthio-propanamide(O.27.68);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-2-methyl-3-methylthio-propanamide(O.2769.);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N,2-dimethyl-3-methylthio-propanamide(O.27.70);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-methyl-3-methylthio-propanamide(O.27.71);N-[4-chloro-2-(3-pyridyl)thiazol-5-yl]-N-ethyl-3-methylthio-propanamide(O.27.72);1-[(6-chloro-3-pyridinyl)methyl]-1,2,3,5,6,7-hexahydro-5-methoxy-7-methyl-8-nitro-imidazo[1,2-a]pyridine(O.27.73);1-[(6-chloropyridin-3-yl)methyl]-7-methyl-8-nitro-1,2,3,5,6,7-hexahydroimidazo[1,2-a]pyridin-5-ol(O.27.74);1-isopropyl-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.75);1-(1,2-dimethylpropyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.76);N,5-dimethyl-N-pyridazin-4-y-1-(2,2,2-trifluoro-1-methyl-ethyl)pyrazole-4-carboxamide(O.27.77);1-[1-(1-cyanocyclopropyl)ethyl]-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.78);N-ethyl-1-(2-fluoro-1-methyl-propyl)-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.79);1-(1,2-dimethylpropyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.80);1-[1-(1-cyanocyclopropyl)ethyl]-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.81);N-methyl--(2-fluoro-1-methyl-propyl]-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.82);1-(4,4-difluorocyclohexyl)-N-ethyl-5-methyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.83);1-(4,4-difluorocyclohexyl)-N,5-dimethyl-N-pyridazin-4-yl-pyrazole-4-carboxamide(O.27.84), N-(1-methylethyl)-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.85); N-cyclopropyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.86); N-cyclohexyl-2-(3-pyridinyl)-2H-indazole-4-carboxamide(O.27.87);2-(3-pyridinyl)-N-(2,2,2-trifluoroethyl)-2H-indazole-4-carboxamide(O.27.88);2-(3-pyridinyl)-N-[(tetrahydro-2-furanyl)methyl]-2H-indazole-5-carboxamide(O.27.89); methyl2-[[2-(3-pyridinyl)-2H-indazol-5-yl]carbonyl]hydrazinecarboxylate(O.27.90);N-[(2,2-difluorocyclopropyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-carboxamide(O.27.91);N-(2,2-difluoropropyl)-2-(3-pyridinyl)-2H-indazole-5-carboxamide(O.27.92);2-(3-pyridinyl)-N-(2-pyrimidinylmethyl)-2H-indazole-5-carboxamide(O.27.93);N-[(5-methyl-2-pyrazinyl)methyl]-2-(3-pyridinyl)-2H-indazole-5-car-boxamide(O.27.94),N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfanyl)propanamide(O.27.95);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-N-ethyl-3-(3,3,3-trifluoropropylsulfinyl)propanamide(O.27.96);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-difluorocyclopropyl)methylsulfanyl]-N-ethyl-propanamide(O.27.97);N-[3-chloro-1-(3-pyridyl)pyrazol-4-yl]-3-[(2,2-difluorocyclopropyl)methylsulfinyl]-N-ethyl-propanamide(O.27.98); sarolaner (O.27.99), lotilaner (O.27.100); in a weight ratioof from 100:1 to 1:100. 12: A fungicidal mixture comprising as activecomponents 1) at least one active compound I as defined in claim 11, oran N-oxide, or an agriculturally useful salt thereof; and as component2) at least one active compound II selected from groups A) to 0) asdefined for component 2) in claim 11, or an N-oxide, or anagriculturally useful salt thereof; and as component 3) at least oneactive compound III selected from groups A) to O) as defined forcomponent 2) in claim 11, or an N-oxide, or an agriculturally usefulsalt thereof; wherein the at least one active compound III of component3) is not identical with the at least one active compound II ofcomponent 2). 13: The mixture according to claim 12, comprising acompound I and a compound II and a further active compound III in asynergistically effective amount. 14: The mixture according to claim 12,comprising a compound I and a compound II in a weight ratio of from100:1 to 1:100, and a compound I and compound III in a weight ratio offrom 100:1 to 1:100. 15: The mixture according to claim 11, wherein R²in compounds of the formula I is hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₆-alkoxy or C₃-C₈-cycloalkyl. 16: The mixtureaccording to claim 11, wherein the component 1) is at least one activecompound I selected from the group consisting ofN-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamide,N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]acetamide,N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]acetamide,N—[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(Z)—N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide,4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one,N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamideor5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one.17: An agrochemical composition, comprising a solvent or solid carrierand a composition according to claim
 11. 18: The agrochemicalcomposition according to claim 17 further comprising seed in an amountof from 1 g to 1000 g active components per 100 kg of seed. 19: A methodfor controlling phytopathogenic harmful fungi, comprising treating thefungi, their habitat or the seed, the soil or the plants to be protectedagainst fungal attack with an effective amount of the mixture of claim11. 20: A method for controlling phytopathogenic harmful fungi,comprising treating the fungi, their habitat or the seed, the soil orthe plants to be protected against fungal attack with an effectiveamount of the composition of claim
 17. 21: The method of claim 19,wherein the mixture comprises as active components 1) at least oneactive compound I as defined in claim 11, or an N-oxide, or anagriculturally useful salt thereof; and as component 2) at least oneactive compound II selected from groups A) to O), or an N-oxide, or anagriculturally useful salt thereof; and as component 3) at least oneactive compound III selected from groups A) to O), or an N-oxide, or anagriculturally useful salt thereof; wherein the at least one activecompound III of component 3) is not identical with the at least oneactive compound II of component 2). 22: The method of claim 19, whereinthe mixture comprises a compound I and a compound II and a furtheractive compound III in a synergistically effective amount. 23: Themethod of claim 19, wherein the mixture comprises a compound I and acompound II in a weight ratio of from 100:1 to 1:100, and a compound Iand compound III in a weight ratio of from 100:1 to 1:100. 24: Themethod of claim 19, wherein R² in compounds of the formula I ishydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-alkoxy orC₃-C₈-cycloalkyl. 25: The method of claim 19, wherein the component 1)is at least one active compound I selected from the group consisting ofN-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(E)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(Z)-methoxyiminomethyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]cyclopropanecarboxamide,N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,2,2-difluoro-N-methyl-2-[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]acetamide,N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]acetamide,N—[(E)-N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N—[(Z)—N-methoxy-C-methyl-carbonimidoyl]-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide,N-allyl-N-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]propanamide,4,4-dimethyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one,N-methyl-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzenecarbothioamideor5-methyl-1-[[4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]phenyl]methyl]pyrrolidin-2-one.